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FDA Inspection 1306942 — Patheon Italia S.p.A

Patheon Italia S.p.A — FEI 3004110157

The FDA completed an inspection of Patheon Italia S.p.A on January 30, 2026 in Ferentino. 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 30, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Ferentino (Italy)

Facility

Other inspections at this facility

  • 1174972 (NAI Tue Jun 14 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1247104 (VAI Fri Feb 25 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1066263 (VAI Fri Sep 21 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1006748 (NAI Mon Oct 31 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 955569 (VAI Wed Dec 16 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources