Quality Record Retention. 5.9.1 The following Supplier quality records related to the production of Rave Gear LLC. products, as applicable, must be retained for a minimum of seven (7) years: Calibration Reports Process Validation Records Design / Document Change Records Customer Complaint Records Corrective and Preventive Action Records
Quality Record Retention. The supplier shall maintain a system with the ability to recall records upon request from Silverado Cable Company, their customer, or US Government. These records may include quality records, inspection/ test records and any certifications pertinent to the product and shall be maintained for a minimum of 7 years after completion of the purchasing contract.
Quality Record Retention. Supplier will maintain appropriate quality records related to the design and production of FMD’s, product or part delivered to INVACARE for a minimum of 10 years after last shipment, unless a longer period is requested by INVACARE. Unless otherwise instructed by XXXXXXXX, such records include batch records, non-conformity records, calibration reports, incoming- in process, end of line inspection and process validation records. At the end of the required retention period, Supplier will contact INVACARE to determine the appropriate disposition of the records (e.g., send to INVACARE, destroy).
Quality Record Retention. Biochrom shall maintain clear, clean and accurate records of results of acceptance activities for each Product delivered to GE Healthcare. These records shall include the test/inspection criteria, revision level of documents/equipment/software used, activities performed (planning, routing or traveler sheets), dates of test/inspection, results and identification of the individual(s) conducting the activities. Where applicable, these records should include a list of the equipment used for test/inspection. All records retained for the Product shall be stored by Biochrom until GE Healthcare notifies Biochrom that the product life has ended.
Quality Record Retention. If the Supplier is required to perform acceptance activities per GE Healthcare written agreement or purchase specification, the Supplier shall maintain records of the acceptance activities for the services performed and/or products and services delivered to GE Healthcare. These records may include as appropriate test/inspection criteria, revision level of documents/equipment/software used, operating procedures (planning, routing or traveler sheets), dates of test/inspection, and the results. The records required shall be retained until GE Healthcare notifies the Supplier that the product life has ended or for a minimum of fifteen (15) years, whichever is longer, unless the required records are submitted to GE Healthcare by written agreement or purchase specification.
Quality Record Retention. The Supplier shall maintain clear, clean and accurate records of results of acceptance activities for each Product delivered to GE Healthcare. These records shall include the test/inspection criteria, revision level of documents/equipment/software used, activities performed (planning, routing or traveler sheets), dates of test/inspection, results and identification of the individual(s) conducting the activities. Where applicable, these records shall include a list of the equipment used for test/inspection. The Supplier shall store all records pertaining to the Product until GE Healthcare notifies the Supplier that the product life has ended and/or GE Healthcare requests the records.
Quality Record Retention. 6.9.1 The following Supplier quality records related to the production of MMS, LLC products, as applicable, must be retained for a minimum of seven (7) years: • Calibration Reports • Process Validation Records • Device History Records (DHR) • Design / Document Change Records • Customer Complaint Records • Corrective and Preventive Action Records
