483
Autocam Medical Devices, LLCAutocam Medical Devices, LLC – FDA 483, Oct 22, 2025
Record Details
Autocam Medical Devices, LLC in Plymouth, MA, a contract manufacturer, was cited for significant deficiencies in its quality system during an FDA inspection. The inspection revealed inadequate procedures for corrective and preventive actions (CAPA), insufficient supplier management controls, and failures in complaint handling documentation. These issues indicate systemic problems in ensuring product quality and compliance.
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