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FDA Inspection 798467 — Octapharma Plasma, Inc. - Norfolk

Octapharma Plasma, Inc. - Norfolk — FEI 3007113703

The FDA completed an inspection of Octapharma Plasma, Inc. - Norfolk on September 11, 2012 in Norfolk, 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
September 11, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Norfolk, VA (United States)

Facility

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FDA data resources