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. 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. 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. Company shall maintain records of inspection, repairs, reworks and tests for the term of the Agreement. Records shall be made available to Microsoft upon request.
Quality Records. The Seller shall maintain quality records as supportive evidence that items identified in this Order conform to specified requirements. Such records shall include, but are not limited to, complete inspection records, product certification, and corrective action for nonconforming product as applicable. All quality records must be maintained for fifteen years from the date of the completion of the Order, unless otherwise specified, in a manner that will retain legibility and prevent damage, deterioration and loss of records.
Quality Records. Xxxxxxxxx-Xxxxx shall maintain original records related to the Manufacture, labeling, packaging, storage and testing of the Products in a limited access area and shall treat such records in accordance with the confidentiality requirements in the Development and Supply Agreement. Access to these records shall be restricted to personnel authorized by Xxxxxxxxx-Xxxxx. Xxxxxxxxx-Xxxxx shall ensure that these records are available to Auxilium upon request within a mutually agreed timeframe. Upon receiving a written request from Auxilium, Xxxxxxxxx-Xxxxx shall transfer to Auxilium copies of all Auxilium -Product related records including but not limited to records relating to critical processes and inspection. If such records have been provided previously, i.e. BPR’s, then an appropriate administrative charge shall apply. Except as required by law, Xxxxxxxxx-Xxxxx shall not release documents for the Products to a third party without the written approval of Auxilium’s QA and Regulatory Departments.
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. 6.6.1 All Quality Control activities shall be recorded and such documentation shall be considered a Quality Record.
Quality Records. All quality documents have to be kept as long as the part is active plus one calendar year. Quality documents (e.g., control charts, test results) must be archived for 3 calendar years. A test certificate according to EN 10204 has to be supplied to SUSPA together with the initial sample inspection report. The required certificate level is 3.1. Deviations to this level have to be agreed separately between SUSPA and the supplier. With series deliveries the test certificates have to be archived by the supplier and have to be shown or handed over to SUSPA on request.
