FDA Inspection 824900 — SANUM-Kehlbeck GmbH & Co. KG

SANUM-Kehlbeck GmbH & Co. KG — FEI 3002128313

The FDA completed an inspection of SANUM-Kehlbeck GmbH & Co. KG on March 26, 2013 in Hoya. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
March 26, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hoya (Germany)