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FDA Inspection
•Mid-America Transplant Services (dba Mid-America Transplant)•April 19, 2019

Mid-America Transplant Services (dba Mid-America Transplant) – FDA Inspection, Apr 19, 2019

Record Details

This FDA Inspection record concerns Mid-America Transplant Services (dba Mid-America Transplant), with an inspection on April 19, 2019, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Mid-America Transplant Services (dba Mid-America Transplant)
Inspection Date
April 19, 2019
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Kathleen B. Swat (FDA Associated Person)
View Company Profile

ID · 5173a6e2-ab2a-4d38-a974-8f22334513fa

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1089056
FDA center
Biologics
Project area
Blood and Blood Products

Other FDA inspections of Mid-America Transplant Services (dba Mid-America Transplant)

5
DateClassificationOfficeProject area
August 23, 2024NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
January 4, 2017NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
October 30, 2014NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
July 25, 2013NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
November 23, 2009NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for Mid-America Transplant Services (dba Mid-America Transplant)
  • FDA Inspection 1247285 - 2024-08-23
  • FDA Inspection 997610 - 2017-01-04
  • FDA Inspection 901726 - 2014-10-30
  • FDA Inspection 841595 - 2013-07-25
  • FDA Inspection 633300 - 2009-11-23

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