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FDA Inspection
•AlloSource Inc•January 10, 2012

AlloSource Inc – FDA Inspection, Jan 10, 2012

Record Details

This FDA Inspection record concerns AlloSource Inc, with an inspection on January 10, 2012, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
AlloSource Inc
Inspection Date
January 10, 2012
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 570f53f5-97e8-4ba8-9400-6cb38b4696e7

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
764470
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

Other FDA inspections of AlloSource Inc

5
DateClassificationOfficeProject area
September 7, 2023NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
July 10, 2019NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
December 9, 2016NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
November 14, 2013NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
June 25, 2010NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for AlloSource Inc
  • FDA Inspection 1217455 - 2023-09-07
  • FDA Inspection 1096121 - 2019-07-10
  • FDA Inspection 994677 - 2016-12-09
  • FDA Inspection 855207 - 2013-11-14
  • FDA Inspection 668744 - 2010-06-25

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