FDA Inspection 913073 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3007960248

The FDA completed an inspection of Octapharma Plasma, Inc. on Jan 16, 2015 in Chesapeake, VA. 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
Jan 16, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Chesapeake, VA (United States)

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