FDA Inspection 1055197 — Apotex Inc.

Apotex Inc. — FEI 3002906944

The FDA completed an inspection of Apotex Inc. on May 10, 2018 in North York. 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
May 10, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
North York (Canada)

Additional Details

Postmarket Adverse Drug Experience (PADE)