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FDA Inspection 1006748 — Patheon Italia S.p.A

Patheon Italia S.p.A — FEI 3004110157

The FDA completed an inspection of Patheon Italia S.p.A on October 31, 2016 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
October 31, 2016
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Ferentino (Italy)

Facility

Other inspections at this facility

  • 1306942 (NAI Fri Jan 30 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 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))
  • 955569 (VAI Wed Dec 16 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources