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 Feb 6, 2018 in Monza. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.