FDA Inspection 1041252 — CeramTec GmbH, Medical Products Division
The FDA completed an inspection of CeramTec GmbH, Medical Products Division on Feb 16, 2018 in Marktredwitz. 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 16, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Marktredwitz (Germany)