Home / Inspections / 1116508

FDA Inspection 1116508 — Octapharma Plasma, Inc. - Norfolk

Octapharma Plasma, Inc. - Norfolk — FEI 3007113703

The FDA completed an inspection of Octapharma Plasma, Inc. - Norfolk on December 5, 2019 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
December 5, 2019
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Norfolk, VA (United States)

Facility

Other inspections at this facility

  • 1297062 (NAI Wed Dec 10 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1008325 (NAI Tue Mar 14 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 903101 (NAI Wed Nov 05 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 798467 (NAI Tue Sep 11 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 741058 (VAI Mon Aug 15 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources