FDA Inspection 1040496 — Octapharma Plasma, Inc

Octapharma Plasma, Inc — FEI 3007387598

The FDA completed an inspection of Octapharma Plasma, Inc on Jan 10, 2018 in Florence, AL. 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
Jan 10, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Florence, AL (United States)