FDA Inspection 907324 — Patheon API Manufacturing Inc

Patheon API Manufacturing Inc — FEI 3001451369

The FDA completed an inspection of Patheon API Manufacturing Inc on Nov 26, 2014 in Greenville, SC. 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
Nov 26, 2014
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Greenville, SC (United States)