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FDA Inspection 1304384 — Catalent Anagni SRL

Catalent Anagni SRL — FEI 3002806546

The FDA completed an inspection of Catalent Anagni SRL on January 20, 2026 in Anagni. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 20, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Anagni (Italy)

Facility

Other inspections at this facility

  • 1278284 (VAI Fri Feb 23 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1172076 (VAI Fri Feb 14 2020 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