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FDA Inspection
•Vitalant Reference and Transfusion Service•June 5, 2019

Vitalant Reference and Transfusion Service – FDA Inspection, Jun 5, 2019

Record Details

This FDA Inspection record concerns Vitalant Reference and Transfusion Service, with an inspection on June 5, 2019, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Vitalant Reference and Transfusion Service
Inspection Date
June 5, 2019
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Amanda B Vega (Issuing Officer)
View Company Profile

ID · 372c43d0-e450-41f4-8ab7-b01c51dd4a6d

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1096131
FDA center
Biologics
Project area
Blood and Blood Products

Other FDA inspections of Vitalant Reference and Transfusion Service

6
DateClassificationOfficeProject area
January 21, 2025Not classifiedPhiladelphia District Office
September 14, 2022NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
May 3, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
May 27, 2014NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
May 16, 2012NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 6 other inspections on the company page
Other documents for Vitalant Reference and Transfusion Service
  • FDA Inspection 1259608 - 2025-01-21
  • FDA Inspection 1179658 - 2022-09-14
  • FDA Inspection 969937 - 2016-05-03
  • FDA Inspection 880162 - 2014-05-27
  • FDA Inspection 782068 - 2012-05-16

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