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FDA Inspection
•Midwest Transplant Network•July 22, 2009

Midwest Transplant Network – FDA Inspection, Jul 22, 2009

Record Details

This FDA Inspection record concerns Midwest Transplant Network, with an inspection on July 22, 2009, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Midwest Transplant Network
Inspection Date
July 22, 2009
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 6bf26cc1-3456-4828-b10f-8c26bda86200

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
598605
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

FDA Citations

3
  1. 21 CFR 1271.215Potential problems with recovery
  2. 21 CFR 1271.180(a)Procedures to meet core CTGP
  3. 21 CFR 1271.190(b)(2)Sewage, trash removal

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Midwest Transplant Network

11
DateClassificationOfficeProject area
April 25, 2025NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
February 19, 2019VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
September 13, 2018NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
August 25, 2016NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
June 2, 2014NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
View all 11 other inspections on the company page
Other documents for Midwest Transplant Network
  • FDA Inspection 1272362 - 2025-04-25
  • FDA Inspection 1079774 - 2019-02-19
  • FDA Inspection 1067227 - 2018-09-13
  • FDA Inspection 983887 - 2016-08-25
  • FDA Inspection 883481 - 2014-06-02

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