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FDA Inspection 621606 — Catalent France Beinheim SA

Catalent France Beinheim SA — FEI 3002808036

The FDA completed an inspection of Catalent France Beinheim SA on September 17, 2009 in Beinheim. 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
September 17, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Beinheim (France)

Facility

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