FDA Inspection 1192265 — AAP Implantate Ag

AAP Implantate Ag — FEI 3001406084

The FDA completed an inspection of AAP Implantate Ag on November 4, 2022 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
November 4, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Berlin (Germany)