FDA Warning Letter — IEM Gmbh
The FDA took a Warning Letter action against IEM Gmbh on February 24, 2012 (Aachen, Germany). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.
Action Details
- Facility
- IEM Gmbh
- Date
- February 24, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Center
- CDRH
- Location
- Aachen (Germany)