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FDA Inspection 853759 — 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, 2013 in Ferentino. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
October 31, 2013
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Ferentino (Italy)

Facility

Other inspections at this facility

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  • 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))

FDA data resources