Home / Inspections / 989834

FDA Inspection 989834 — Catalent Germany Eberbach GmbH

Catalent Germany Eberbach GmbH — FEI 3002808098

The FDA completed an inspection of Catalent Germany Eberbach GmbH on March 18, 2016 in Eberbach. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 18, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Eberbach (Germany)

Facility

Other inspections at this facility

  • 1255823 (VAI Fri Feb 02 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1106613 (NAI Fri Sep 06 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1048712 (NAI Fri Mar 02 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 850147 (NAI Thu Sep 12 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 818378 (NAI Fri Feb 08 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources