FDA Inspection 1041862 — Patheon Italia S.p.A.

Patheon Italia S.p.A. — FEI 3003065803

The FDA completed an inspection of Patheon Italia S.p.A. on February 6, 2018 in Monza. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 6, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Monza (Italy)