FDA Warning Letter — Siegfried Hameln GmbH

Case 363318 — FEI 3002807877

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.