FDA Inspection 556932 — Catalent Pharma Solutions, LLC

Catalent Pharma Solutions, LLC — FEI 1000122400

The FDA completed an inspection of Catalent Pharma Solutions, LLC on Dec 9, 2008 in Winchester, KY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 9, 2008
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Winchester, KY (United States)

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