FDA Warning Letter — Oertel Medical GmbH

Case 303918 — FEI 3002809480

The FDA took a Warning Letter action against Oertel Medical GmbH on June 11, 2012 (Tuttlingen, Germany). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Oertel Medical GmbH
Date
June 11, 2012
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Tuttlingen (Germany)