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FDA Inspection
•Octapharma Plasma Inc•August 29, 2024

Octapharma Plasma Inc – FDA Inspection, Aug 29, 2024

Record Details

This FDA Inspection record concerns Octapharma Plasma Inc, with an inspection on August 29, 2024, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Octapharma Plasma Inc
Inspection Date
August 29, 2024
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
People
  • Kish Bolden (Issuing Officer)
  • Steen N. Graham (Issuing Officer)
View Company Profile

ID · 02cffa56-07c0-46df-9718-1a7f7ca48c58

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1250909
FDA center
Biologics
Project area
Blood and Blood Products

Other FDA inspections of Octapharma Plasma Inc

6
DateClassificationOfficeProject area
July 23, 2026NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
April 22, 2026NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
March 30, 2026NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
March 19, 2026NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
March 11, 2026NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 6 other inspections on the company page
Other documents for Octapharma Plasma Inc
  • FDA Inspection 1329120 - 2026-07-23
  • FDA Inspection 1317018 - 2026-04-22
  • FDA Inspection 1312082 - 2026-03-30
  • FDA Inspection 1310204 - 2026-03-19
  • FDA Inspection 1282432 - 2026-03-11

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