FDA Warning Letter — Bayer AG

Case 68548 — FEI 3002808084

The FDA took a Warning Letter action against Bayer AG on August 5, 2009 (Bergkamen, Germany). The action was issued by CDER and concerns drugs products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Bayer AG
Date
August 5, 2009
Fiscal Year
2009
Product Type
Drugs
Center
CDER
Location
Bergkamen (Germany)