FDA Inspection 1250909 — Octapharma Plasma Inc

Octapharma Plasma Inc — FEI 3020752193

The FDA completed an inspection of Octapharma Plasma Inc on Aug 29, 2024 in Pennsauken, 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
Aug 29, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Pennsauken, NJ (United States)