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FDA Inspection
•Reproductive Medicine Institute•June 9, 2026

Reproductive Medicine Institute – FDA Inspection, Jun 9, 2026

Record Details

This FDA Inspection record concerns Reproductive Medicine Institute, with an inspection on June 9, 2026, issued by the Chicago District Office, covering biologics.

Company
Reproductive Medicine Institute
Inspection Date
June 9, 2026
Product Type
Biologics
Office
Chicago District Office
People
  • David A. Moore (Investigator)
  • Zoey A. Trombley (FDA Personnel)
View Company Profile

ID · cad92f77-b2be-448c-9168-4f11ca6dfe8f

Inspection Facts

Inspection number
1321232
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies
Outcome
Form 483 issued, view the record

FDA Citations

1
  1. 21 CFR 1271.90(c)Eligibility not required--warning labels

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Reproductive Medicine Institute

6
DateClassificationOfficeProject area
August 21, 2023NAICenter for Biologics Evaluation and ResearchVaccines and Allergenic Products
June 19, 2018NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
May 12, 2016NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
May 19, 2014NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
November 29, 2011NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
View all 6 other inspections on the company page
Other documents for Reproductive Medicine Institute
  • FDA Inspection 1216427 - 2023-08-21
  • FDA Inspection 1057831 - 2018-06-19
  • FDA Inspection 969650 - 2016-05-12
  • FDA Inspection 879502 - 2014-05-19
  • FDA Inspection 754960 - 2011-11-29

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Contact
New York Office:
370 Jay Street 7th Floor
Brooklyn, NY 11201
Scranton Office:
Scranton Enterprise Center, Suite 217
201 Lackawanna Avenue
Scranton, PA, 18503
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🇪🇺+48 532-447-507
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