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FDA Inspection
•University of Michigan Center for Reproductive Medicine•February 14, 2019

University of Michigan Center for Reproductive Medicine – FDA Inspection, Feb 14, 2019

Record Details

This FDA Inspection record concerns University of Michigan Center for Reproductive Medicine, with an inspection on February 14, 2019, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
University of Michigan Center for Reproductive Medicine
Inspection Date
February 14, 2019
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
People
  • Amy S. Graf (Issuing Officer)
  • Erma Zaimova
View Company Profile

ID · 6248c785-f367-4952-89b5-f8f619d45efe

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1084090
FDA center
Biologics
Project area
Blood and Blood Products

Other FDA inspections of University of Michigan Center for Reproductive Medicine

6
DateClassificationOfficeProject area
June 2, 2025Not classifiedDetroit District Office
March 20, 2018VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
January 7, 2016NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
July 25, 2013VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
June 22, 2011NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
View all 6 other inspections on the company page
Other documents for University of Michigan Center for Reproductive Medicine
  • FDA Inspection 1272476 - 2025-06-02
  • FDA Inspection 1044924 - 2018-03-20
  • FDA Inspection 959777 - 2016-01-07
  • FDA Inspection 841672 - 2013-07-25
  • FDA Inspection 731053 - 2011-06-22

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