FDA Inspection 792665 — Catalent France Beinheim SA

Catalent France Beinheim SA — FEI 3002808036

The FDA completed an inspection of Catalent France Beinheim SA on Jul 13, 2012 in Beinheim. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jul 13, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Beinheim (France)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.