Quality Records. The Vendor shall maintain the following Quality Records on site as a condition of purchase for a minimum of 10 Years unless otherwise specified. The Vendor shall create a job traveler (operation sheet) for each lot manufactured with Part Number and Revision Levels, specified signatures and inspection verification (stamp or signature) for each lot manufactured. Full material traceability must be maintained for each lot (traveler) shipped and must include a signed off Final Inspection (Form 3) indicating the final acceptance of each lot manufactured and supplied to AGP. Quality Records also includes the supplier’s programs and tool data sheets which are kept on file at site. 100% Inspection is required by Vendor and lot sampling is not permitted without direct written consent from the Director of Quality at AGP. Noted records do not need to be shipped unless specifically requested by PO requirement, but must be kept on file for 10 years unless otherwise specified. If Key Characteristics Control is required a 100% inspection shall apply and the actual data (measurements taken) shall be forwarded 100% with each shipment. All gages used by Vendor on AGP parts must be calibrated and traceable to National Institute of Standards Technology (NIST).
Quality Records. Quality records contain the results of inspections which have been carried out. The Supplier shall constantly maintain records relating to the inspection results for important and critical criteria and shall make these avail- able to the Customer on request. If required by special agreements or by the ordering documentation, the test results relating to relevant criteria shall be included together with the consignment.
Quality Records. The Supplier shall have procedures for identifying quality records (such as material test reports or inspection records) to be maintained and/or retained. The quality record procedures shall indicate the personnel responsible for retrieval, retention, and disposition of quality records.
Quality Records. SANMINA-SCI shall have a system for the collection and maintenance of quality assurance records. A document describing such system shall be submitted to CUSTOMER (for information and approval) prior to beginning work. Quality assurance records, whether written or electronic, shall be adequately protected from deterioration or damage, and shall be made available for CUSTOMER’s inspection on reasonable notice. SANMINA-SCI shall maintain all quality assurance records pertaining to this Agreement during the term of this Agreement and for a period of one (1) year following any expiration or termination of this Agreement.
Quality Records. Under its QMS, the Supplier is obliged to document the product and process specifications (e.g. test and measurement values, process parameters, etc.) in their entirety and archive all the relevant documents (quality records). The Supplier is obliged to document the history of all key parts from the beginning of development/production, so that any changes can be traced consistently against the original date of use. The Supplier shall update this history after every change to the date and submit it to GG. The Supplier is obliged to keep these quality records for 15 years. After this period, the Supplier shall submit the documents to GG free of charge. The destruction of these quality records requires the prior written consent of GG. The Supplier shall xxxxx XX or a customer of GG access to the quality records for verification purposes at any time on request.
Quality Records. 8.4.1 All Quality Control activities shall be recorded and such documentation shall be considered a Quality Record.
Quality Records. Company shall maintain records of inspection, repairs, reworks and tests for the term of the Agreement. Records shall be made available to MS upon request 14.3 *
Quality Records. PDEX will maintain manufacturing quality records for all Products. PDEX will make those documents available within a reasonable time period at the request of MAKO or within 48 hours in the event of any mandatory audit of MAKO by a notified body or the FDA.
Quality Records. Supplier shall establish and maintain procedures for identification, collection, indexing, filing, storage, maintenance, and disposition of all quality records. As examples, these records may include raw data or control charts, for critical/identified process parameters, and records of all inspection and test activity to provide objective evidence that products have passed acceptance criteria. Records shall be maintained for time periods as agreed to between the Supplier and KORNIT. A listing of all quality records, with the retention period defined, must be maintained. Product Quality Addendums may contain additional requirements regarding the management of quality records. SUPPLIER QUALITY REQUIREMENTS DOCUMENT Page l of 19 Revision: A1 Date: 02/04/15 Author: Xxxxxx.H 11 Standard Compliance Requirements
Quality Records. The types of records that will be generated and maintained by Consultant during the execution of this QA program shall be outlined.
