FDA Warning Letter — IEM Gmbh

Case 276156 — FEI 1000628323

The FDA took a Warning Letter action against IEM Gmbh on Feb 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
Feb 24, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Aachen (Germany)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.