FDA Inspection 1055436 — Autocam Medical Devices, LLC

Autocam Medical Devices, LLC — FEI 3001644153

The FDA completed an inspection of Autocam Medical Devices, LLC on May 18, 2018 in Plymouth, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 18, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Plymouth, MA (United States)