FDA Inspection 1238005 — Patheon Italia S.p.A.

Patheon Italia S.p.A. — FEI 3003065803

The FDA completed an inspection of Patheon Italia S.p.A. on January 26, 2023 in Monza. 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
January 26, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Monza (Italy)

Additional Details

Mutual Recognition Agreement (MRA)