FDA Inspection 1003014 — Biomet France SARL
The FDA completed an inspection of Biomet France SARL on Feb 3, 2017 in Valence Cedex 9. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Feb 3, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Valence Cedex 9 (France)