FDA Inspection 1059538 — Octapharma USA, Inc.

Octapharma USA, Inc. — FEI 3004146033

The FDA completed an inspection of Octapharma USA, Inc. on Jun 20, 2018 in Paramus, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 20, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Paramus, NJ (United States)

Additional Details

Sponsor, Contract Research Organization