FDA Inspection 1202777 — Octapharma Plasma Inc

Octapharma Plasma Inc — FEI 3017830194

The FDA completed an inspection of Octapharma Plasma Inc on April 7, 2023 in Dayton, 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
April 7, 2023
Fiscal Year
2023
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Dayton, OH (United States)