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FDA Inspection 654570 — Catalent Germany Eberbach GmbH

Catalent Germany Eberbach GmbH — FEI 3002808098

The FDA completed an inspection of Catalent Germany Eberbach GmbH on March 5, 2010 in Eberbach. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 5, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Eberbach (Germany)

Facility

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