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质量协议英文版

1. CONTRACT PARTNERS

This Master Quality Agreement is concluded between:

Hereinafter referred to as "Customer) and:

also acting on behalf of its affiliated and associated companies, hereinafter referred to as “SUBCONTRACTOR(SUPPLIER)".

2. PERIOD OF VALIDITY

This Master Quality Agreement is effective after the date of acceptance by both CUSTOMER and

SUBCONTRACTOR(SUPPLIER).

This Master Quality Agreement is valid until the end of usage of the products (parts) by CUSTOMER, included the product lifetime.

3. TABLE OF CONTENTS

1. CONTRACT PARTNERS (1)

2. PERIOD OF VALIDITY (1)

3. TABLE OF CONTENTS (2)

4. REFERENCED DOCUMENT (2)

5. PURPOSE (3)

6. ZERO-DEFECTS............................................................................................................... 错误!未定义书签。

7. APPLICABLE DOCUMENTS (4)

7.1. Product specification (4)

7.2. Quality agreement documents (5)

7.3. Standards (5)

7.4. Order of precedence (5)

7.5. Environment. (5)

8. MUTUAL ACCESS, VERIFICATION AND CONFIDENTIALITY (7)

9. QUALIFICATION (7)

9.1. System (8)

9.2. Process (8)

9.3. Product (8)

10. SAFETY (9)

11. APPLICATION VALIDATION (9)

12. CHANGE CONTROL (10)

13. PROCESS CONTROL (10)

14. PRODUCT INSPECTION, MONITORING AND REPORTING (12)

15. QUALITY SPECIFICATION (12)

16. PPM MANAGEMENT (12)

16.1. Complaints and handling of rejects. (13)

16.2. Costs. (13)

16.3. Production line. (14)

17. HANDLING OF REJECTS (14)

18. SHELF LIFE AND WARRANTY (14)

19. TRACKING AND TRACING (15)

20. SIGNATURE SHEET (16)

4. REFERENCED DOCUMENT

The format of this Master Quality Agreement is documented in the standards system

5. PURPOSE

The purpose of this Master Quality Agreement (MQA) is to establish the quality system elements, the working relationship and the feedback systems between CUSTOMER and SUBCONTRACTOR(SUPPLIER) for products to be procured by CUSTOMER from SUBCONTRACTOR(SUPPLIER). The Master Quality Agreement establishes also the basic elements, which are required and aimed on the continuous improvement of the product conformity and reliability performance.

This document, as a memorandum of understanding, does not affect the terms and conditions set out by the Supply Agreement.

The Master Quality Agreement shall be used in conjunction with a Quality Data Sheet (QDS) or quality specification on product level.

6. Quality Target (Defect rate definition)

Both SUBCONTRACTOR(SUPPLIER) and CUSTOMER are committed to the principle of Annual Quality Target, in which all product defects and failures as well as other quality discrepancies, which provoke the need for complaints, are to be considered as unacceptable. The improvement to the target should following the roadmap of agreed annual and quarter milestones. Both parties will actively co-operate to investigate the causes of failure and the implementation of corrective- as well as preventive actions and generally assist each other in the achievement of mutually beneficial opportunities for quality improvement.

As evidence of the SUBCONTRACTOR(SUPPLIER)’s commitment to the Quality Target goal, SUBCONTRACTOR(SUPPLIER) agrees to supply products in accordance with the conformity and reliability targets as specified in the Quality Data Sheet (QDS) or quality specification.

2005 Q1 Q2 Q3 Q4

Active Box 2500 2000 1000 800

Passive Box 2000 1000 500 500

Wireless 2500 2500 1500 1000

7. APPLICABLE DOCUMENTS

7.1. Product specification

The product specification is a document containing at least the following information:

-Product identification.

-Functional description, diagrams, drawings, etc. covering all aspects required for an optimal application.

-Functional parameters and characteristics with limiting values, measuring methods and conditions unless not stated in the Quality Data Sheet (QDS).

-Physical dimensions and tolerances

critical dimensions are marked with X or XX or or the CUSTOMER customer's symbol

-The identification as safety component (if applicable)

-Safety characteristics (if applicable)

-Environmental demand: see 7.5.

-Packing methods and quantities per packing unit.

Quantity per reel, layer, staple or box : ...... pieces

-Total reels; layers, staples or boxes in 1 unit packaging : x pieces

- 1 unit packaging can be a big carton box, pallet or boxpallet

-

Marked on every box :

* Production date

* Traceability information

* ERP codenumber

* Total quantity in the box

Please fill in the Packaging Data Sheet for reach code number send to us. See sheet

document ref. Nb Log001 in annex 1

When pieces are shipped by air, boxes have to be covered with plastic foil, or they

have to be in a plastic bag to avoid that the boxes get wet by condension.

When pieces are shipped by sea, the pieces inside the box must be in a plastic bag

together with moisture absorbent. The packaging must ensure that the pieces don’t

get damaged during transport also by stacking (piling) pallets on each other.

Before CUSTOMER will procure any product, both parties will agree on the product and packing specification.

SUBCONTRACTOR(SUPPLIER) is responsible for ensuring that any product shipped to CUSTOMER meets the requirements of the product specification.

The valid product specification document will be specified; reference will be made either to SUBCONTRACTOR(SUPPLIER)’s specification or to a CUSTOMER specification confirmed by SUBCONTRACTOR(SUPPLIER).

7.2. Quality agreement documents

Master Quality Agreement (MQA):

The MQA contains all basic quality aspects as mentioned in this document. It does not cover product- or product category related requirements. The MQA is signed only once and is valid for all product categories delivered by SUBCONTRACTOR(SUPPLIER).

7.3. Standards

The latest revision of the international standards, to which reference is made in the drawing, form a part of the quality agreement to the extent specified herein.

7.4. Order of precedence

Where there are conflicting requirements, documents shall rank in the following order of authority:

-the product specification, clause 7.1 of this agreement

-quality standaard or specification.

-the Supply Agreement

-the Master Quality Agreement, (other item agreed in this document)

-the IEC(Q) specifications to which reference is made

-any other international document to which reference is made

- a national standard

7.5. Environment.

SUBCONTRACTOR(SUPPLIER) warrants that all his articles supplied to CUSTOMER, CUSTOMER's customers and/or its affiliated companies do not and will not contain Banned Substances from the List of Banned Substances (as below) or, if present, are below the declaration threshold concentration mentioned in this List.

Treshold concentration

PPM (mg/kg)

Cadmium and -compounds 5

Mercury and -compounds 2

Asbestos (all types) 10

CFCs, Chlorofluorcarbons 0

HCFCs, Hydrogenated chlorofluorcarbons 0

CHCs, Chlorinated hydrocarbons 0

PBBEs, poly brominated biphenyl ethers 10

PBBs, poly brominated biphenyls 10

PCBs, poly chlorinated biphenyls 10

PCTs, poly chlorinated triphenyls 10

PCP, Pentachlorophenol 10

PVC and PVC blends 1000

(only for consumer packaging)

Packaging materials sold to CUSTOMER must be free of PVC and -blends.

The chemical content of each article should be known. The environmental certificate and the list of banned and relevant substances must be completed and signed for each new article, even if the article does not contain such substances. See certificate and list (.annex 1) Relevant substances are not forbidden but should be avoided if possible, since they are considered to be removed in case of recycling of the article.

One certificate can be used for several articles if all the following conditions are met: the articles contain the same materials, are manufactured in the same process and the content of listed substances is approximately the same (within 10%).

CUSTOMER can indicate in the quality specification that no certificate is necessary for subsequent articles of the same “family”. The symbol means that, in the case of compounds, the concentration of the chemical element should be calculated, not the compound. For substances without the symbol, the amount of the compound has to be given.

PPM means part per million or milligram per kilogram. 1 ppm = 0.0001 %

The environmental data, including weight, are related to the article itself, excluding packaging. Only the listed substances, which are present in the article, should be indicated, not the substances used in the manufacturing or cleaning process.

Recycle symbols:

- Cardboard primary packaging and paper (instructions) for consumer articles: according to DIN 6120 (3 folded arrows), from 50 grams on.

- Plastic primary packaging for consumer articles: according to DIN 6120 (appropriate number within 3 closed arrows, plastic type abbreviation underneath), from 5 grams on or bags > 3 dm2. - Other plastic parts (not for packaging): according ISO 11469 (3 closed arrows with plastic type abbreviation underneath between > <), from 25 grams on. If only small areas are available, the arrows can be omitted.

Packaging of the articles.

A returnable packaging should be considered if economically achievable. CUSTOMER joins several organisations like the Pallet Pool. If certain conditions are met,

SUBCONTRACTOR(SUPPLIER)s can also join these organisations for returnable packaging. In case of non-returnable packaging, preference is given to recyclable materials. In decreasing order of preference: cardboard, metals, non-treated wood. Other materials are considered as not recyclable Authorities (Pest Control) can request to use certain chemicals (pesticides) for protection of wood. In this case wood is considered as non-recyclable.

8. MUTUAL ACCESS, VERIFICATION AND CONFIDENTIALITY

SUBCONTRACTOR(SUPPLIER)'s manufacturing and distribution facilities will be accessible to CUSTOMER representatives in order to verify whether SUBCONTRACTOR(SUPPLIER) observes the obligations and activities on the basis of this agreement. CUSTOMER’s manufacturing facilities will be accessible to SUBCONTRACTOR(SUPPLIER)’s representatives to observe the handling and processing of SUBCONTRACTOR(SUPPLIER)’s products.

In both cases the normal courtesies of prior notification and agreement will be observed.

Both parties agree to keep in strictest confidence and not use for itself or disclosure to any third party any confidential and propriety information disclosed by one of the parties during the course of audits, visits and discussions, unless agreed otherwise between SUBCONTRACTOR(SUPPLIER) and CUSTOMER.

9. QUALIFICATION

9.1. System

SUBCONTRACTOR(SUPPLIER) will take care of the appropriate ISO 9000-2000 (LAST VERSION) way of working of its quality system. This system will ensure that the appropriate procedures are in place to assure conformance to the requirements of quality specification. Moreover the system will provide for the prevention and early detection of discrepancies and for timely corrective- and preventive actions. CUSTOMER is entitled upon prior notification to visit SUBCONTRACTOR(SUPPLIER) to perform a quality system audit on the basis of the appropriate ISO 9000-2000 document.

According to actual situation, SUBCONTRACTOR(SUPPLIER)s are under obligation to set up other

Relevant quality or environmental/sustainability system base on customer requirement, such as ISO/TS16949, ISO14001, etc.

9.2. Process

SUBCONTRACTOR(SUPPLIER) will have a documented process description. This description will ensure that products are developed, produced and distributed resulting in products meeting the requirements of the product specification and the product specific quality agreement. CUSTOMER is entitled upon prior notification to visit SUBCONTRACTOR(SUPPLIER) to perform a process audit.

9.3. Product

The purpose of product qualification is to establish that the product has the capability to meet the requirements of the product specification, before delivery of the product; the product has to be qualified by CUSTOMER.

SUBCONTRACTOR(SUPPLIER) and CUSTOMER will agree well in advance a joint qualification program before deliveries will commence. This qualification program may include: ? Measuring system studies

?Engineering approval

?Process flowchart

?Process FMEA

?Appearances approval report

?Sample product

?Dimensional results

?Test results

?Control plan

Process capability study

SUBCONTRACTOR(SUPPLIER) will, on request, provide CUSTOMER with qualification samples, which are representative for the future products to be delivered. On request of CUSTOMER, SUBCONTRACTOR(SUPPLIER) will supply the information, which provides the evidence that the product complies with the requirements as outlined in the qualification program. After qualification, the SUBCONTRACTOR(SUPPLIER) will not introduce any product and/or significant manufacturing process change without notifying CUSTOMER well in advance, see clause 12. CUSTOMER reserves the right to refuse deliveries and is entitled to restart the qualification procedure, in those cases where it is proven that products are showing non-conformance to the requirements. See also ISO TS 16949 (LAST VERSION) procedures.

10. SAFETY

Safety products are defined as products for which safety certification by one or more institutions, like BSI, VDE, Femko/Demko/Nemko/Semko, UL, CSA, etc. is required. SUBCONTRACTOR(SUPPLIER) is responsible for acquisition and distribution to CUSTOMER of these listings.

Safety defects will be considered as critical defects. Every product will be submitted to inspection on critical defects during SUBCONTRACTOR(SUPPLIER)’s manufacturing process. SUBCONTRACTOR(SUPPLIER) will immediately alarm CUSTOMER upon detection of any product with a critical defect and the risk exists that products with critical defects have been delivered to CUSTOMER. A joint action plan will be initiated. If CUSTOMER identifies any safety defect, SUBCONTRACTOR(SUPPLIER) will be alarmed and a joint action plan will be initiated.

11. APPLICATION VALIDATION

CUSTOMER may request SUBCONTRACTOR(SUPPLIER) to validate the application of his product in the CUSTOMER or the CUSTOMER's customer’s product, assembly or set. The final responsibility for the application of SUBCONTRACTOR(SUPPLIER)’s product in the CUSTOMER product, assembly or set always remains with CUSTOMER.

12. CHANGE CONTROL

1. Change of Designs or specifications

CUSTOMER may, effective upon notice to SUBCONTRACTOR(SUPPLIER), change SUBCONTRACTOR(SUPPLIER)’s designs or specifications at any time prior to shipment of corresponding products or receipt of corresponding services. If any such change affects the prices or delivery schedules of products or services, an equitable adjustment shall be made provided that SUBCONTRACTOR(SUPPLIER) promptly makes a written claim for an adjustment prior to shipment of products or provision of services. If the parties are unable to agree upon the amount of the adjustment, CUSTOMER may, without any liability to SUBCONTRACTOR(SUPPLIER), terminate the Purchase Order or the Purchase Agreement as to all products and/or services affected.

2. Approval of process or design changes.

SUBCONTRACTOR(SUPPLIER) shall not, without the prior written consent of CUSTOMER make any changes affecting products, including process or design changes, changes to geographical relocation of manufacturing processes, or process step discontinuances affecting the performance (whether specified or not), the mechanical form or fit, the environmental compatibility or chemical characteristics, the life, reliability or quality of products or changes that have significant impact upon SUBCONTRACTOR(SUPPLIER)S quality system.

The change request will be accompanied by information, which explains the reason for the change, and information, which provides the evidence that the product still meets the requirements of the product specification and the quality specification/standard.

13. PROCESS CONTROL

Statistical Process Control will be applied throughout SUBCONTRACTOR(SUPPLIER)’s process.

Process capability indexes (Cpk's) will be established for the critical product parameters and the correlating process parameters. The critical product parameters will be established in mutual agreement.

PPK and CpK should be measured according to customer requirement

An acceptable level of preliminary capability must be determined prior to submission for all characteristics designated by the customer or SUBCONTRACTOR(SUPPLIER). Safety, Key, or Significant characteristics can be evaluated using variables (measured) data. The purpose of this requirement is to determine if the production process is likely to produce products that will meet the customer’s req uirements. The conventional procedure for estimating process capability is described below.

Other methods more appropriate for certain processes or products may be substituted with prior customer approval.

Preliminary process studies are short-term and will not predict the effects of time and variation in people, materials, methods, equipment, measurement systems, and environment. Even for these short-term studies, it is important to collect and analyse the data in the order they are produced using control charts.

It is advisable to perform a measurement system analysis (Gage R & R, accuracy, linearity, and stability studies) to understand how measurement error is affecting the study measurements. (Refer to the Measurement System Analysis instruction).

For those characteristics that can be studied using X-bar and R charts, a short-term study should be based on 25 more subgroups of data containing at least a total of 100 individual readings.

Note that the particular sampling plan used can influence the appearance of stability.

The control chart should be examined for signs of instability; corrective actions should be taken. If stability cannot be achieved, CUSTOMER has to be contacted and determine appropriate action.

The preliminary data requirement may be replaced by longer-term results from the same or similar process, with customer concurrence. For certain processes, alternative analytical tools such, as individual and moving range charts are appropriate.

Processes that Appear unstable. Depending on the nature of the instability, the process may not meet customer requirements. Special causes should be identified, evaluated and, wherever possible, eliminated. Use 100% inspection and increased sampling until ongoing stability is demonstrated or until the customer is satisfied. Process improvement must be given a high priority and documented in a corrective action plan. A revised Control Plan for these interim actions must be reviewed with and approved by the customer.

If acceptable process capability cannot be obtained by the part submission promise date, a corrective action plan and an interim revised Control plan (normally providing for 100% inspection) must be developed by the SUBCONTRACTOR(SUPPLIER) and approved by the

responsible part approval activity. Typical corrective actions include: process improvement, tooling changes and changes to the customer’s enigineering requirements.

14. PRODUCT INSPECTION, MONITORING AND REPORTING SUBCONTRACTOR(SUPPLIER) will inspect all products or perform sampling inspection on batches of products prior to shipment to CUSTOMER and will systematically monitor the reliability performance of his products and will report appropriate details at the request of CUSTOMER. SUBCONTRACTOR(SUPPLIER) will immediately alarm CUSTOMER upon detection of potential problems, which may lead to a deterioration of CUSTOMER perceived conformity or reliability levels. Verbal notifications will be confirmed in writing and supported by regular status reports until corrective- and preventive actions are in place. The detection of a potential safety hazard by either CUSTOMER or SUBCONTRACTOR(SUPPLIER) will be cause for immediate joint notification and action.

To avoid degradation of the product, the SUBCONTRACTOR(SUPPLIER) must check min. 1 or 2 times a year the total specification and test all the requirements of the product.

CUSTOMER will send resident engineer and inspectors in SUBCONTRACTOR(SUPPLIER)s to monitor on going

Quality, the sampling inspection or full check action will be taken on final products according to actual situation, and after qualification release, SUBCONTRACTOR(SUPPLIER) can deliver to upper level customer.

15. QUALITY SPECIFICATION

The quality requirements will be specified on the drawing and on the Quality requirement. When a critical defect is found, the lot or batch will immediately be rejected. re defined as catastrophic failures, being failures which are both sudden and complete (IEC 50- 191).

16. PPM MANAGEMENT

An essential element of PPM management is PPM co-operation. The purpose of PPM co-operation is to achieve overall quality improvement, whereby the ultimate goal is ZERO DEFECTS. For certain products, CUSTOMER may start-up a PPM co-operation with SUBCONTRACTOR(SUPPLIER) and gives feedback on a regular base. The ways of working

will be as described below. The line rejects will be returned to SUBCONTRACTOR(SUPPLIER) accompanied by an analysis request form with product data, reject data and failure data. SUBCONTRACTOR(SUPPLIER) will analyse the rejects and establish the net reject level,

which is the level for which SUBCONTRACTOR(SUPPLIER) can be held responsible. The analysis results of both CUSTOMER and SUBCONTRACTOR(SUPPLIER) will be used to achieve further line fall-off reduction. To review progress and

plan further actions, the SUBCONTRACTOR(SUPPLIER) must send from each returned PPM batch an action plan with the reason of the failure, action to avoid the failure. When we send this (returned batch) weekly or monthly please take care that this (action plan) will be send to us

also weekly or monthly.

16.1. Complaints and handling of rejects.

SUBCONTRACTOR(SUPPLIER) will be informed about costs for sorting out bad pieces. If SUBCONTRACTOR(SUPPLIER) doesn’t agree with these costs (must be done within 24 hours) the parts must be sorted out by the SUBCONTRACTOR(SUPPLIER) and he must deliver new pieces, depending on our planning and mutual agreement.

SUBCONTRACTOR(SUPPLIER) will inform us immediately by fax, e-mail and by phone about his possible in-between stock and what he is going to do with it.

SUBCONTRACTOR(SUPPLIER) has 2 workdays to give a first reaction on the quality complaint. SUBCONTRACTOR(SUPPLIER) needs to describe the actions taken and the results of these actions. (see also clause 17.

Together with the first following delivery, SUBCONTRACTOR(SUPPLIER) needs to inform CUSTOMER by fax or e-mail with an explanation about this delivery: either the SUBCONTRACTOR(SUPPLIER) has sorted out his in-between stock, and than he has to

inform CUSTOMER about the results or he has taken actions and delivered out of a new production run. After reject the SUBCONTRACTOR(SUPPLIER) has to send along with the new production run, a measuring report with the dimensions or requirments that have caused

the problem.

According to actual situation, CUSTOMER may require the Subcontractor to add special marks. Back charge of the costs involved will be as arranged per Supply Agreement.

16.2. Production line.

If defects (defects > than 2x PPM target) are identified in CUSTOMER production lines (line rejects), they will be confirmed by visual inspection for damages and/or defects and functional re-testing in a mutually agreed testing system. This to verify that the products are defective, happens on the cost of SUBCONTRACTOR(SUPPLIER).

If the problem is not solved after 4 months, SUBCONTRACTOR(SUPPLIER) has to pay the costs x 150 %

If the problem is not solved after 6 months, CUSTOMER will give no more new business to the SUBCONTRACTOR(SUPPLIER) and has the right to solve the problem with all reasonable means.

17. HANDLING OF REJECTS

The analysis reports will answer at least the following questions:

-why did the product pass SUBCONTRACTOR(SUPPLIER)'s test and inspections?

-how will SUBCONTRACTOR(SUPPLIER) prevent it passing the tests and inspections?

-when will SUBCONTRACTOR(SUPPLIER) implement this?

-what is the root cause of the defect?

-why did this root cause happen?

-how will SUBCONTRACTOR(SUPPLIER) prevent it to happen again?

-when will SUBCONTRACTOR(SUPPLIER) implement this?

-SUBCONTRACTOR(SUPPLIER) will subsequently follow up the corrective- and preventive action plans by reporting monthly (unless otherwise agreed), this until

completion of the actions. In the case of "no-fault" found,

SUBCONTRACTOR(SUPPLIER) will contact CUSTOMER to come to a joint

decision on appropriate follow-up actions.

CUSTOMER requires the SUBCONTRACTOR(SUPPLIER)s to use the 8D report to

reply on any reject and complaint.

18. SHELF LIFE AND WARRANTY

Both SUBCONTRACTOR(SUPPLIER) and CUSTOMER will apply the principle of FIRST-IN FIRST-OUT to stock rotation. The shelf life will be specified in the Quality Data Sheet. However, as CUSTOMER wants to benefit to the maximum extend of SUBCONTRACTOR(SUPPLIER)’s

continuous improvement program, CUSTOMER wants to receive fresh products, i.e. the production date of the products upon receipt at CUSTOMER premises will not be older than the time period as specified in the Quality Data Sheet.

In case the products are older, CUSTOMER is entitled to return the products freight collect for replacement by fresh products. Other options may be agreed between CUSTOMER and SUBCONTRACTOR(SUPPLIER). SUBCONTRACTOR(SUPPLIER) warrants the conformity of each product to the product specification during the shelf life period.

19. TRACKING AND TRACING

SUBCONTRACTOR(SUPPLIER) will maintain a product tracking system capable of identifying production batches in the manufacturing and supply chain. A record of product design, quality, manufacturing technology and environmental conformance will be maintained for a minimum period of 2 years unless otherwise specified by CUSTOMER's customer..

20. SIGNATURE SHEET

For CUSTOMER: For

SUBCONTRACTOR(SUPPLIER):

............... ..............

(name) (name)

............... ...............

(function) (function)

............... ...............

(signature) (signature)

............... ...............

(date) (date)

Company stamp Company stamp

ANNEX 1 : ENVIRONMENTAL CERTIFICATE FOR ARTICLES

The information will be treated CONFIDENTIALLY.

SUPPLIER OR SUBCONTRACTOR(SUPPLIER) :

Article (family) :

Return completed to :

If valid tick off:

¨SUPPLIER OR SUBCONTRACTOR(SUPPLIER) warrants that the above indicated articles as supplied by it to Customer and/or its affiliated companies do not contain

banned nor relevant substances from the Customer List of Banned and Relevant

Substances (as attached) or, if present, are below the threshold concentration levels

mentioned in this List.

¨SUPPLIER OR SUBCONTRACTOR(SUPPLIER) confirms that the above indicated articles as supplied by it to Customer and/or its affiliated companies do not contain

banned substances from the Customer List of Banned and Relevant Substances or, if

present, are below the threshold concentration levels mentioned in this List, but the

articles do contain relevant substances with concentrations above the threshold values mentioned in this List. (Please indicate substance(s) concerned, and concentration(s) in ppm value (mg/kg) on the attached List.)

SUPPLIER OR SUBCONTRACTOR(SUPPLIER) warrants that no other substances are present in the supplied articles or, if present, are below the threshold concentrations as mentioned in the above List, as submitted to the SUPPLIER OR

SUBCONTRACTOR(SUPPLIER).

¨SUPPLIER OR SUBCONTRACTOR(SUPPLIER) confirms that the above indicated articles as supplied by it to Customer and/or its affiliated companies do contain banned substances from the Customer List of Banned an Relevant Substances with

concentrations above the threshold concentration levels mentioned in this List. (Please indicate banned and relevant substance(s) concerned, and concentration(s) in ppm

value (mg/kg) on the attached List.)

SUPPLIER OR SUBCONTRACTOR(SUPPLIER) warrants that no other substances are present in the supplied articles or, if present, are below the threshold concentrations as mentioned in the above List, as submitted to the SUPPLIER OR

SUBCONTRACTOR(SUPPLIER).

Name : (SUBCONTRACTOR(SUPPLIER)'s Company Stamp)

Function :

Date :

质量保证及服务协议

质量保证及服务协议 编号: 共页 甲方: 乙方: 签订地点: 签订日期:

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