FDA Inspection 1160499 — Octapharma Plasma Inc

Octapharma Plasma Inc — FEI 3016248752

The FDA completed an inspection of Octapharma Plasma Inc on December 30, 2021 in Augusta, GA. 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
December 30, 2021
Fiscal Year
2022
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Augusta, GA (United States)