FDA Warning Letter — Bayer AG

Case 526288 — FEI 3002806462

The FDA took a Warning Letter action against Bayer AG on November 14, 2017 (Leverkusen, 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
November 14, 2017
Fiscal Year
2018
Product Type
Drugs
Center
CDER
Location
Leverkusen (Germany)