FDA Inspection 1085178 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3007302994

The FDA completed an inspection of Octapharma Plasma, Inc. on Mar 8, 2019 in Orange Park, FL. 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
Mar 8, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Orange Park, FL (United States)