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FDA Inspection 791773 — Octapharma Plasma Inc

Octapharma Plasma Inc — FEI 3006804255

The FDA completed an inspection of Octapharma Plasma Inc on July 12, 2012 in Cleveland, 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
July 12, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Cleveland, OH (United States)

Facility

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FDA data resources