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FDA Inspection
•Versiti Illinois, Inc.•February 6, 2023

Versiti Illinois, Inc. – FDA Inspection, Feb 6, 2023

Record Details

This FDA Inspection record concerns Versiti Illinois, Inc., with an inspection on February 6, 2023, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Versiti Illinois, Inc.
Inspection Date
February 6, 2023
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Paul M. Chefor (Investigator)
View Company Profile

ID · c2871eb2-684d-4d0e-8025-d3e9882ff1ad

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1197407
FDA center
Biologics
Project area
Vaccines and Allergenic Products

Other FDA inspections of Versiti Illinois, Inc.

6
DateClassificationOfficeProject area
December 18, 2018NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
December 21, 2016NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 24, 2015NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
December 16, 2013NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
January 11, 2012NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 6 other inspections on the company page
Other documents for Versiti Illinois, Inc.
  • FDA Inspection 1078416 - 2018-12-18
  • FDA Inspection 995353 - 2016-12-21
  • FDA Inspection 915626 - 2015-02-24
  • FDA Inspection 859433 - 2013-12-16
  • FDA Inspection 762668 - 2012-01-11

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