FDA Inspection 763237 — Octapharma Plasma, Inc

Octapharma Plasma, Inc — FEI 3007387598

The FDA completed an inspection of Octapharma Plasma, Inc on Dec 30, 2011 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
Dec 30, 2011
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Florence, AL (United States)