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FDA Inspection 1247104 — Patheon Italia S.p.A

Patheon Italia S.p.A — FEI 3004110157

The FDA completed an inspection of Patheon Italia S.p.A on February 25, 2022 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: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 25, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ferentino (Italy)

Additional Details

Mutual Recognition Agreement (MRA)

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))
  • 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