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FDA Inspection 664473 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3006402207

The FDA completed an inspection of Octapharma Plasma, Inc. on May 26, 2010 in Petersburg, VA. 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
May 26, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Petersburg, VA (United States)

Facility

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FDA data resources