FDA Inspection 818378 — Catalent Germany Eberbach GmbH

Catalent Germany Eberbach GmbH — FEI 3002808098

The FDA completed an inspection of Catalent Germany Eberbach GmbH on February 8, 2013 in Eberbach. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Food/Cosmetics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 8, 2013
Fiscal Year
2013
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Eberbach (Germany)