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FDA Inspection
•Versiti Indiana, Inc.•August 4, 2023

Versiti Indiana, Inc. – FDA Inspection, Aug 4, 2023

Record Details

This FDA Inspection record concerns Versiti Indiana, Inc., with an inspection on August 4, 2023, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Versiti Indiana, Inc.
Inspection Date
August 4, 2023
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Lesley Mae P. Lutao (Investigator)
View Company Profile

ID · d4eb9770-d445-458a-b273-6bfbeee80699

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1214844
FDA center
Biologics
Project area
Blood and Blood Products

Other FDA inspections of Versiti Indiana, Inc.

6
DateClassificationOfficeProject area
March 11, 2025NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
November 1, 2017NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 2, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
June 24, 2014NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
September 18, 2012VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 6 other inspections on the company page
Other documents for Versiti Indiana, Inc.
  • FDA Inspection 1264016 - 2025-03-11
  • FDA Inspection 1032128 - 2017-11-01
  • FDA Inspection 957611 - 2016-02-02
  • FDA Inspection 884440 - 2014-06-24
  • FDA Inspection 799301 - 2012-09-18

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