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FDA Inspection
•University of Cincinnati Center For Reproductive Health•November 22, 2010

University of Cincinnati Center For Reproductive Health – FDA Inspection, Nov 22, 2010

Record Details

This FDA Inspection record concerns University of Cincinnati Center For Reproductive Health, with an inspection on November 22, 2010, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
University of Cincinnati Center For Reproductive Health
Inspection Date
November 22, 2010
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 2a672fe8-8ed2-4ddb-ae0c-50838e4ced16

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
698506
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

FDA Citations

3
  1. 21 CFR 1271.75(a)(1)Risk factors, clinical evidence
  2. 21 CFR 1271.90(c)Eligibility not required--warning labels
  3. 21 CFR 1271.50(a)Responsible person to determine, document

Full citation text and observation details available on the Dashboard.

Other FDA inspections of University of Cincinnati Center For Reproductive Health

10
DateClassificationOfficeProject area
February 26, 2026Not classifiedCincinnati District OfficeHuman Cellular, Tissue, and Gene Therapies
June 27, 2023NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
November 20, 2019NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
October 26, 2017NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
November 6, 2014NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
View all 10 other inspections on the company page
Other documents for University of Cincinnati Center For Reproductive Health
  • FDA Inspection 1305410 - 2026-02-26
  • FDA Inspection 1209064 - 2023-06-27
  • FDA Inspection 1111182 - 2019-11-20
  • FDA Inspection 1030555 - 2017-10-26
  • FDA Inspection 902859 - 2014-11-06

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