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FDA Inspection
•Versiti Illinois Inc•January 14, 2010

Versiti Illinois Inc – FDA Inspection, Jan 14, 2010

Record Details

This FDA Inspection record concerns Versiti Illinois Inc, with an inspection on January 14, 2010, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Versiti Illinois Inc
Inspection Date
January 14, 2010
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · f3445b68-2892-4c2a-93a1-28d5ed1665d9

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
638368
FDA center
Biologics
Project area
Blood and Blood Products

FDA Citations

2
  1. 21 CFR 606.100(c)Thorough investigations
  2. 21 CFR 606.100(b)(19)Notification of consignees re: antibody test results

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Versiti Illinois Inc

7
DateClassificationOfficeProject area
January 16, 2025NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
September 15, 2022NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
January 16, 2018NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
December 9, 2015NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
May 29, 2013NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 7 other inspections on the company page
Other documents for Versiti Illinois Inc
  • FDA Inspection 1259068 - 2025-01-16
  • FDA Inspection 1180930 - 2022-09-15
  • FDA Inspection 1045130 - 2018-01-16
  • FDA Inspection 952598 - 2015-12-09
  • FDA Inspection 833390 - 2013-05-29

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