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FDA Inspection
•AHN Center for Reproductive Medicine•April 2, 2013

AHN Center for Reproductive Medicine – FDA Inspection, Apr 2, 2013

Record Details

This FDA Inspection record concerns AHN Center for Reproductive Medicine, with an inspection on April 2, 2013, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
AHN Center for Reproductive Medicine
Inspection Date
April 2, 2013
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 29d8cf66-5655-440c-a2ce-9a5a4f7a31e2

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
824130
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

FDA Citations

2
  1. 21 CFR 1271.47(b)Review and approval of procedures
  2. 21 CFR 1271.47(a)Testing, screening, donor eligibility procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of AHN Center for Reproductive Medicine

5
DateClassificationOfficeProject area
January 10, 2024NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 9, 2022NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
August 24, 2017NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
May 14, 2015NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
August 5, 2010VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for AHN Center for Reproductive Medicine
  • FDA Inspection 1227204 - 2024-01-10
  • FDA Inspection 1162459 - 2022-02-09
  • FDA Inspection 1024633 - 2017-08-24
  • FDA Inspection 925853 - 2015-05-14
  • FDA Inspection 674147 - 2010-08-05

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