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FDA Inspection 850147 — Catalent Germany Eberbach GmbH

Catalent Germany Eberbach GmbH — FEI 3002808098

The FDA completed an inspection of Catalent Germany Eberbach GmbH on September 12, 2013 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
September 12, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Eberbach (Germany)

Facility

Other inspections at this facility

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  • 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))
  • 989834 (NAI Fri Mar 18 2016 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