FDA Inspection 1171459 — Octapharma Plasma Inc

Octapharma Plasma Inc — FEI 3017887952

The FDA completed an inspection of Octapharma Plasma Inc on Apr 28, 2022 in Aurora, CO. 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
Apr 28, 2022
Fiscal Year
2022
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Aurora, CO (United States)