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FDA Inspection
•East Tennessee IVF and Andrology Center•October 17, 2008

East Tennessee IVF and Andrology Center – FDA Inspection, Oct 17, 2008

Record Details

This FDA Inspection record concerns East Tennessee IVF and Andrology Center, with an inspection on October 17, 2008, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
East Tennessee IVF and Andrology Center
Inspection Date
October 17, 2008
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 53f11126-c0d6-467f-88be-dcde5d068813

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
543422
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

Other FDA inspections of East Tennessee IVF and Andrology Center

5
DateClassificationOfficeProject area
September 30, 2024Not classifiedNew Orleans District Office
June 14, 2018NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
December 2, 2015NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
November 25, 2013NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
April 14, 2011NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for East Tennessee IVF and Andrology Center
  • FDA Inspection 1251394 - 2024-09-30
  • FDA Inspection 1069825 - 2018-06-14
  • FDA Inspection 950469 - 2015-12-02
  • FDA Inspection 857576 - 2013-11-25
  • FDA Inspection 721561 - 2011-04-14

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