FDA Warning Letter — SANUM-Kehlbeck GmbH & Co. KG

Case 406594 — FEI 3002128313

The FDA took a Warning Letter action against SANUM-Kehlbeck GmbH & Co. KG on April 11, 2014 (Hoya, Germany). The action was issued by CDER and concerns drugs products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
SANUM-Kehlbeck GmbH & Co. KG
Date
April 11, 2014
Fiscal Year
2014
Product Type
Drugs
Center
CDER
Location
Hoya (Germany)