FDA Inspection 818868 — IEM Gmbh
The FDA completed an inspection of IEM Gmbh on January 24, 2013 in Aachen. 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
- January 24, 2013
- Fiscal Year
- 2013
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Aachen (Germany)