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FDA Inspection 983376 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 2377733

The FDA completed an inspection of Octapharma Plasma, Inc. on August 4, 2016 in Gretna, LA. 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
August 4, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Gretna, LA (United States)

Facility

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FDA data resources