FDA Warning Letter — Dornier Medtech GmbH

Case 203432 — FEI 3002806833

The FDA took a Warning Letter action against Dornier Medtech GmbH on August 26, 2011 (Wessling, Germany). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Dornier Medtech GmbH
Date
August 26, 2011
Fiscal Year
2011
Product Type
Devices
Center
CDRH
Location
Wessling (Germany)