FDA Inspection 1198516 — Octapharma Plasma Inc

Octapharma Plasma Inc — FEI 3014248297

The FDA completed an inspection of Octapharma Plasma Inc on February 14, 2023 in Akron, OH. 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
February 14, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Akron, OH (United States)