FDA Inspection 865407 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 3006402207

The FDA completed an inspection of Octapharma Plasma, Inc. on January 31, 2014 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
January 31, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Petersburg, VA (United States)