FDA Warning Letter — Siegfried Hameln GmbH

Case 363318 — FEI 3002807877

The FDA took a Warning Letter action against Siegfried Hameln GmbH on December 21, 2012 (Hameln, 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
Siegfried Hameln GmbH
Date
December 21, 2012
Fiscal Year
2013
Product Type
Drugs
Center
CDER
Location
Hameln (Germany)