FDA Inspection 1160862 — Octapharma Plasma Inc

Octapharma Plasma Inc — FEI 3017096853

The FDA completed an inspection of Octapharma Plasma Inc on Oct 27, 2021 in Riverdale, MD. 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 27, 2021
Fiscal Year
2022
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Riverdale, MD (United States)