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FDA Inspection 818220 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3006188513

The FDA completed an inspection of Octapharma Plasma, Inc. on January 25, 2013 in Springfield, IL. 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
January 25, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Springfield, IL (United States)

Facility

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FDA data resources