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FDA Inspection
•Vitalant•August 7, 2024

Vitalant – FDA Inspection, Aug 7, 2024

Record Details

This FDA Inspection record concerns Vitalant, with an inspection on August 7, 2024, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Vitalant
Inspection Date
August 7, 2024
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
People
  • Elyshia Q. Danaher (Issuing Officer)
  • Shelley H. Beausoleil (Issuing Officer)
View Company Profile

ID · f300122d-3b5f-4420-8224-64f4b3e47fc9

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1247163
FDA center
Biologics
Project area
Blood and Blood Products

Other FDA inspections of Vitalant

6
DateClassificationOfficeProject area
November 27, 2018NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
December 7, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
January 14, 2015NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
December 12, 2012NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
April 19, 2011NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 6 other inspections on the company page
Other documents for Vitalant
  • FDA Inspection 1076433 - 2018-11-27
  • FDA Inspection 999732 - 2016-12-07
  • FDA Inspection 911710 - 2015-01-14
  • FDA Inspection 810328 - 2012-12-12
  • FDA Inspection 720616 - 2011-04-19

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