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FDA Inspection
•Huntington Reproductive Center Medical Group•May 25, 2011

Huntington Reproductive Center Medical Group – FDA Inspection, May 25, 2011

Record Details

This FDA Inspection record concerns Huntington Reproductive Center Medical Group, with an inspection on May 25, 2011, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Huntington Reproductive Center Medical Group
Inspection Date
May 25, 2011
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 334b485b-dd07-4354-9db4-648f9793fa89

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
726254
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

FDA Citations

1
  1. 21 CFR 1271.85(c)Reproductive cells or tissues

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Huntington Reproductive Center Medical Group

4
DateClassificationOfficeProject area
June 1, 2023NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
January 19, 2018NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
February 2, 2016NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
November 8, 2012NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for Huntington Reproductive Center Medical Group
  • FDA Inspection 1207182 - 2023-06-01
  • FDA Inspection 1043586 - 2018-01-19
  • FDA Inspection 982064 - 2016-02-02
  • FDA Inspection 807674 - 2012-11-08

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