FDA Inspection 756823 — ACTIVAERO GMBH
The FDA completed an inspection of ACTIVAERO GMBH on Nov 24, 2011 in Gemunden (Wohra). 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
- Nov 24, 2011
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Gemunden (Wohra) (Germany)