FDA Inspection 854883 — Octapharma Plasma, Inc

Octapharma Plasma, Inc — FEI 3007387598

The FDA completed an inspection of Octapharma Plasma, Inc on Nov 8, 2013 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
Nov 8, 2013
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Florence, AL (United States)