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FDA Inspection
•Octapharma Plasma, Inc. - Norfolk•December 5, 2019

Octapharma Plasma, Inc. - Norfolk – FDA Inspection, Dec 5, 2019

Record Details

This FDA Inspection record concerns Octapharma Plasma, Inc. - Norfolk, with an inspection on December 5, 2019, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Octapharma Plasma, Inc. - Norfolk
Inspection Date
December 5, 2019
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 9635dc2b-9194-490b-a9b2-6e1da4be41d7

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1116508
FDA center
Biologics
Project area
Blood and Blood Products

Other FDA inspections of Octapharma Plasma, Inc. - Norfolk

5
DateClassificationOfficeProject area
December 10, 2025NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
March 14, 2017NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
November 5, 2014NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
September 11, 2012NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 15, 2011VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
Other documents for Octapharma Plasma, Inc. - Norfolk
  • FDA Inspection 1297062 - 2025-12-10
  • FDA Inspection 1008325 - 2017-03-14
  • FDA Inspection 903101 - 2014-11-05
  • FDA Inspection 798467 - 2012-09-11
  • FDA Inspection 741058 - 2011-08-15

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