FDA Warning Letter — Boehringer Ingelheim Pharma GmbH & Co. KG

Case 393563 — FEI 3002806556

The FDA took a Warning Letter action against Boehringer Ingelheim Pharma GmbH & Co. KG on May 6, 2013 (Ingelheim am Rhein, 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
Boehringer Ingelheim Pharma GmbH & Co. KG
Date
May 6, 2013
Fiscal Year
2013
Product Type
Drugs
Center
CDER
Location
Ingelheim am Rhein (Germany)