FDA Inspection 841994 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 2977477

The FDA completed an inspection of Octapharma Plasma, Inc. on July 26, 2013 in Las Vegas, NV. 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
July 26, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Las Vegas, NV (United States)