FDA 483 - Mid South Precision, Inc. - October 25, 2021

An FDA inspection of Mid South Precision, Inc., a contract manufacturer in Murfreesboro, TN, identified three significant issues. The firm failed to adequately establish and implement procedures for supplier management, properly document acceptance activities in device history records, and initiate corrective and preventive actions for identified nonconformances. These observations indicate deficiencies in the firm's quality system.