FDA Inspection 1201064 — Octapharma Plasma Inc

Octapharma Plasma Inc — FEI 3017899821

The FDA completed an inspection of Octapharma Plasma Inc on March 9, 2023 in Memphis, TN. 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
March 9, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Memphis, TN (United States)