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FDA Inspection 1172076 — Catalent Anagni SRL

Catalent Anagni SRL — FEI 3002806546

The FDA completed an inspection of Catalent Anagni SRL on February 14, 2020 in Anagni. 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
February 14, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Anagni (Italy)

Additional Details

Mutual Recognition Agreement (MRA)

Facility

Other inspections at this facility

  • 1304384 (NAI Tue Jan 20 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1278284 (VAI Fri Feb 23 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1063186 (VAI Fri Mar 31 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 952513 (VAI Fri Nov 20 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 841312 (VAI Tue Jul 02 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources