FDA Inspection 1253473 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3011502580

The FDA completed an inspection of Octapharma Plasma, Inc. on Oct 24, 2024 in Decatur, GA. 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
Oct 24, 2024
Fiscal Year
2025
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Decatur, GA (United States)