FDA Inspection 753156 — IEM Gmbh
The FDA completed an inspection of IEM Gmbh on Oct 21, 2011 in Aachen. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.
Inspection details
- Classification
- Official Action Indicated (OAI)
- End Date
- Oct 21, 2011
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Aachen (Germany)