FDA Inspection 1286076 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3014027617

The FDA completed an inspection of Octapharma Plasma, Inc. on October 8, 2025 in West Palm Beach, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 8, 2025
Fiscal Year
2026
Product Type
Biologics
Project Area
Blood and Blood Products
Location
West Palm Beach, FL (United States)