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FDA Inspection
•The Center For Human Reproduction d.b.a. American Infertility of New York, P.C.•February 15, 2013

The Center For Human Reproduction d.b.a. American Infertility of New York, P.C. – FDA Inspection, Feb 15, 2013

Record Details

This FDA Inspection record concerns The Center For Human Reproduction d.b.a. American Infertility of New York, P.C., with an inspection on February 15, 2013, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
The Center For Human Reproduction d.b.a. American Infertility of New York, P.C.
Inspection Date
February 15, 2013
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · 22165ea5-4824-45e6-9103-07467d90f72e

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
818244
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

FDA Citations

2
  1. 21 CFR 1271.55(d)(2)Accurate, indelible, legible
  2. 21 CFR 1271.47(a)Procedures for all other requirements

Full citation text and observation details available on the Dashboard.

Other FDA inspections of The Center For Human Reproduction d.b.a. American Infertility of New York, P.C.

6
DateClassificationOfficeProject area
May 1, 2024VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
April 11, 2022NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
August 9, 2018NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
March 3, 2017VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
January 14, 2015VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
View all 6 other inspections on the company page
Other documents for The Center For Human Reproduction d.b.a. American Infertility of New York, P.C.
  • FDA Inspection 1237978 - 2024-05-01
  • FDA Inspection 1167650 - 2022-04-11
  • FDA Inspection 1065664 - 2018-08-09
  • FDA Inspection 1009224 - 2017-03-03
  • FDA Inspection 909449 - 2015-01-14

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