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FDA Inspection
•Rejoice IVF Lab, LLC•January 12, 2023

Rejoice IVF Lab, LLC – FDA Inspection, Jan 12, 2023

Record Details

This FDA Inspection record concerns Rejoice IVF Lab, LLC, with an inspection on January 12, 2023, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Rejoice IVF Lab, LLC
Inspection Date
January 12, 2023
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Christopher J. Adams (Issuing Officer)
View Company Profile

ID · e49d314e-0de5-4670-b111-891bd40833a6

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1195299
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

Other FDA inspections of Rejoice IVF Lab, LLC

5
DateClassificationOfficeProject area
August 18, 2026NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
March 9, 2017NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
February 23, 2015NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
November 9, 2011NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
October 26, 2009NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for Rejoice IVF Lab, LLC
  • FDA Inspection 1332790 - 2026-08-18
  • FDA Inspection 1003978 - 2017-03-09
  • FDA Inspection 915669 - 2015-02-23
  • FDA Inspection 753550 - 2011-11-09
  • FDA Inspection 625018 - 2009-10-26

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