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FDA Inspection 556932 — Catalent Pharma Solutions, LLC

Catalent Pharma Solutions, LLC — FEI 1000122400

The FDA completed an inspection of Catalent Pharma Solutions, LLC on December 9, 2008 in Winchester, KY. 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
December 9, 2008
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Winchester, KY (United States)

Facility

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FDA data resources