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FDA Inspection
•Cooper Institute for Advanced Reproductive Medicine•December 22, 2014

Cooper Institute for Advanced Reproductive Medicine – FDA Inspection, Dec 22, 2014

Record Details

This FDA Inspection record concerns Cooper Institute for Advanced Reproductive Medicine, with an inspection on December 22, 2014, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Cooper Institute for Advanced Reproductive Medicine
Inspection Date
December 22, 2014
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 9fbb5de9-06d0-4c49-9228-fb9a11c1ae26

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
907753
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

FDA Citations

1
  1. 21 CFR 1271.80(b)Specimen collections not timely

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Cooper Institute for Advanced Reproductive Medicine

5
DateClassificationOfficeProject area
October 29, 2025Not classifiedDallas District OfficeHuman Cellular, Tissue, and Gene Therapies
November 16, 2023OAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
December 9, 2022OAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
July 19, 2021OAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
April 26, 2017NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for Cooper Institute for Advanced Reproductive Medicine
  • FDA Inspection 1289322 - 2025-10-29
  • FDA Inspection 1223634 - 2023-11-16
  • FDA Inspection 1192782 - 2022-12-09
  • FDA Inspection 1146456 - 2021-07-19
  • FDA Inspection 1017306 - 2017-04-26

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