SUPPLIER Form #: 007 AUDIT QUESTIONNAIRE



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1.0 BACKGROUND INFORMATION Company Name: Company Address: Phone Number: Fax Number: Number of years in business: Number of employees: Annual Sales in Dollars: Size of Facility in Square Feet: Name of Senior Quality Representative: Title: Number of personnel in Quality / Inspection Department: This survey completed by: Title: Describe the Products or services your company provides Dynomax: If your organization has been certified to an ISO, Automotive, or Aerospace standard, simply complete Section 1.0 and return the survey along with a photocopy of your certificate and a photocopy of the revision page of your current quality policy manual. 2.0 QUALITY POLICY 2.1 Does your company have a documented Quality Policy which defines the objectives for a commitment to quality? YES NO 2.2 Has the Quality Policy been approved and signed by company management? YES NO 2.3 Do you have a documented Quality System? YES NO 2.4 Is your Quality System based on any recognized national, government, YES NO or military standard? 2.4.1 If so, which standard(s)? Date of last audit? Last audit performed by: Page 1 of 8

2.0 QUALITY POLICY (con't) 2.5 Has your system been audited and approved by any recognized organization within the past 2 years? YES NO 2.5.1 If so, please provide the name of certifying company, date and standard you have been approved to? 2.5.2 Please attach a photocopy of certification documents 2.6 Would you allow Dynomax AND OUR CUSTOMERS to perform an on-site audit? YES NO 3.0 RESPONSIBILITY AND AUTHORITY 3.1 Do you have an organizational chart or other form of responsibility definition? YES NO 3.2 Does the department responsible for Quality report directly to the President? YES NO 3.3 Does the department responsible for Quality have the authority to control further processing and delivery of product until the unsatisfactory condition has YES NO been corrected? 4.0 RESOURCES AND PERSONNEL 4.1 Do inspection / verification activities include: Incoming Inspection YES NO In-Process Inspection YES NO Final Inspection YES NO 4.2 Are personnel performing product verifications adequately trained? YES NO 4.2.1 Do you keep records of such training? YES NO 4.3 Are personnel performing and verifying special processes certified? YES NO (i.e.. plating, soldering, etc. ) 4.4 Are personnel performing inspection / verification independent of those having direct responsibility of the work being performed? YES NO Page 2 of 8

5.0 QUALITY MANUAL 5.1 Is the Quality Manual approved by company management? YES NO 5.2 Is the Quality Manual reviewed and updated annually? YES NO 5.3 Does the Quality Manual include a Revision Page and a Table of Contents? (If so, please attach a copy of each) YES NO 5.4 Are internal audits performed with results documented and reported to management? YES NO 6.0 CONTRACT REVIEW 6.1 Are all customer contracts / purchase orders reviewed prior to start of work? YES NO 6.2 Is the department responsible for Quality involved in this review? YES NO 6.3 If a problem arises which may impact the quality, quantity, or delivery of the contract, is the customer notified? YES NO 6.4 Is production suspended until written response is obtained from customer? YES NO 7.0 DOCUMENT CONTROL 7.1 Are products manufactured to: Dynomax drawings and specifications? YES NO Your own drawings and specifications? YES NO 7.2 Is there a step in the process to verify that current revisions of YES NO applicable drawings and specifications are available prior to production? 7.3 Are OBSOLETE drawings removed from production areas or, are they YES NO very clearly marked? 7.4 Are Dynomax drawing and specification changes reviewed for impact on YES NO machine settings or other applicable production controls? Page 3 of 8

8.0 PURCHASING 8.1 Are sources for purchased parts controlled by an approved suppliers list? YES NO 8.2 Are your suppliers monitored for performance? YES NO 8.3 Are your suppliers surveyed or evaluated? YES NO 8.0 PURCHASING (con't) 8.4 Do your purchasing documents reference designations of: YES NO TYPE, CLASS, GRADE, STYLE, DOCUMENT REVISION, AND DATE REQUIRED as applicable to the item being purchased? 8.5 Do you perform source inspections at your supplier's facilities? YES NO 8.6 Does the department responsible for Quality review your purchasing documents YES NO which give directions to your suppliers? 8.7 Do you periodically verify supplier's testing for compliance on raw materials? YES NO 8.7.1 If yes, how and at what frequency? 9.0 PRODUCT IDENTIFICATION AND TRACEABILITY 9.1 Are final assemblies traceable to the operator performing each step YES NO of the assembly? 9.2 Are the components of final assemblies traceable back to their raw materials YES NO at any stage of production? Page 4 of 8

10.0 PROCESS CONTROL 10.2 Are written instructions provided for each operation or assembly stage? YES NO 10.3 Is a process traveler, routing ticket, or batch card system employed YES NO for identification? 10.4 Are applicable customer specifications clearly noted? YES NO 10.5 Is non-conforming in-process material identified and kept separate from YES NO acceptable product? 11.0 RECEIVING INSPECTION 11.1 Are there written instructions for receiving inspection? YES NO 11.2 Does receiving inspection compare product received to your own YES NO purchase documents? 11.3 Do you require your suppliers to supply documented evidence as required YES NO by your customers or applicable specifications? 11.4 Review of above documentation is part of the receiving inspection process? YES NO 11.5 Are functional test performed as required? YES NO 11.6 Is non-conforming product identified, separated, and documented by YES NO appropriate review personnel? 11.7 Is product allowed to be used without required testing being performed? YES NO 11.7.1 If yes, is there a "Product Recall" system in place? YES NO Page 5 of 8

12.0 INSPECTION, MEASURING AND TEST EQUIPMENT SUPPLIER Form #: 007 12.1 Has all equipment used in the evaluation of final product been identified, YES NO calibrated, and verified at prescribed intervals? 12.2 Is calibration of equipment traceable to N.I.S.T.? YES NO 12.3 Is the calibration system controlled by written instructions? YES NO 12.4 Is calibrated equipment identified with a tag noting the next due date YES NO and an identifying number? 12.5 Is equipment used if it is "out of calibration"? YES NO 12.6 If yes, is product re-inspected or recalled after equipment has been re-calibrated? YES NO 13.0 INSPECTION AND TEST STATUS 13.1 While in process, is product identified with the following information: Name of product YES NO Applicable drawing / specification revision? YES NO Operator identification YES NO Type of Inspection or testing to be performed YES NO Stamp or initials indicating completion of operation YES NO 13.2 Are industry accepted (i.e. MIL-STD-105, or ANSI / ASQC Z1.4-1993) YES NO sampling plans used? 13.3 Do you use SPC techniques for process control? YES NO 14.0 CONTROL OF NON-CONFORMING PRODUCT 14.1 Is non-conforming product identified and separated to prevent improper YES NO use or shipmement? 14.2 Is non-conforming product documented, evaluated, and dispositioned? YES NO 14.3 Are your customers involved is the disposition of non-conforming material? YES NO Page 6 of 8

14.0 CONTROL OF NON-CONFORMING PRODUCT (con't) SUPPLIER Form #: 007 14.4 Are non-conformance documents periodically reviewed for tend formation? YES NO 14.5 Are customer non-conformances documented and addressed until the YES NO customer is satisfied? 14.6 Do you have a Supplier Corrective Action System? YES NO 14.7 Do you have an Internal Corrective Action System? YES NO 14.8 Are corrective actions verified for completion and effectiveness? YES NO 14.9 Is reworked / repaired product re-inspected prior to use or shipment? YES NO 15.0 HANDLING, STORAGE, PACKAGING, AND DELIVERY 15.1 Are there written instructions for packaging of final products for shipping? YES NO 15.2 Is there adequate protection of products against damage or deterioration during: Assembly / production YES NO Packaging YES NO Shipping YES NO 15.3 Is applicable shelf life clearly identified on package and supporting documentation? YES NO 15.4 Are Customers notified immediately upon discovery that a delivery will be late? YES NO Page 7 of 8

16.0 COMMENTS 16.1 Please use this area for additional comments which will explain any un-answered questions or will provide support for the aspects of your system which are considered the most critical 17.0 CONCLUSION 17.1 This area for Dynomax internal use only. Reviewed by: Date: Status Completion Date Attachments APPROVED Yes No CONDITIONALLY APPROVED Yes No CORRECTIVE ACTION REQUESTED Yes No NOT-APPROVED Yes No Page 8 of 8