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FDA Inspection 792665 — Catalent France Beinheim SA

Catalent France Beinheim SA — FEI 3002808036

The FDA completed an inspection of Catalent France Beinheim SA on July 13, 2012 in Beinheim. 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
July 13, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Beinheim (France)

Facility

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