FDA Inspection 1017003 — AAP Implantate Ag
The FDA completed an inspection of AAP Implantate Ag on May 17, 2017 in Berlin. 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 17, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Berlin (Germany)