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FDA Inspection 1302124 — Catalent France Beinheim SA

Catalent France Beinheim SA — FEI 3002808036

The FDA completed an inspection of Catalent France Beinheim SA on November 25, 2022 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
November 25, 2022
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Beinheim (France)

Additional Details

Mutual Recognition Agreement (MRA)

Facility

Other inspections at this facility

  • 1174733 (VAI Thu Oct 29 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1022739 (VAI Fri Jul 21 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 878382 (NAI Thu Mar 20 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 792665 (NAI Fri Jul 13 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 621606 (VAI Thu Sep 17 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources