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FDA Inspection
•Center for Reproductive Health Fertility Laboratory of Nashville•June 30, 2022

FDA Inspection 1173190 - Center for Reproductive Health Fertility Laboratory of Nashville - June 30, 2022

Record Details

This FDA Inspection record concerns Center for Reproductive Health Fertility Laboratory of Nashville, with an inspection on June 30, 2022, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Center for Reproductive Health Fertility Laboratory of Nashville
Inspection Date
June 30, 2022
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · e6fc0f79-946a-4b24-97ae-573c0d69fe6d

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1173190
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

Other FDA inspections of Center for Reproductive Health Fertility Laboratory of Nashville

6
DateClassificationOfficeProject area
February 23, 2024VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
March 1, 2019VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
July 21, 2017VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 12, 2015NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
May 6, 2011NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
View all 6 other inspections on the company page
Other documents for Center for Reproductive Health Fertility Laboratory of Nashville
  • FDA Inspection 1230770 - 2024-02-23
  • FDA Inspection 1080855 - 2019-03-01
  • FDA Inspection 1019153 - 2017-07-21
  • FDA Inspection 913833 - 2015-02-12
  • FDA Inspection 725380 - 2011-05-06

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