FDA Inspection 947265 — Patheon Softgels Inc

Patheon Softgels Inc — FEI 3004436627

The FDA completed an inspection of Patheon Softgels Inc on Oct 5, 2015 in Greensboro, NC. 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
Oct 5, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Greensboro, NC (United States)

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