FDA Inspection 1286384 — AAP Implantate Ag

AAP Implantate Ag — FEI 3001406084

The FDA completed an inspection of AAP Implantate Ag on September 11, 2025 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
September 11, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Berlin (Germany)