FDA Inspection 1247489 — Octapharma Plasma Inc

Octapharma Plasma Inc — FEI 3017754857

The FDA completed an inspection of Octapharma Plasma Inc on Jul 17, 2024 in York, PA. 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
Jul 17, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
York, PA (United States)