FDA Inspection 932190 — CeramTec GmbH, Medical Products Division
The FDA completed an inspection of CeramTec GmbH, Medical Products Division on Jun 10, 2015 in Plochingen. 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
- Jun 10, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Plochingen (Germany)