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FDA Inspection
•Hudson Valley Fertility, PLLC•August 19, 2016

Hudson Valley Fertility, PLLC – FDA Inspection, Aug 19, 2016

Record Details

This FDA Inspection record concerns Hudson Valley Fertility, PLLC, with an inspection on August 19, 2016, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Hudson Valley Fertility, PLLC
Inspection Date
August 19, 2016
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · c3f3600d-1ee2-4625-8f13-9ae9b963b781

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
985373
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

FDA Citations

2
  1. 21 CFR 1271.200(d)Inspected routinely
  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 Hudson Valley Fertility, PLLC

5
DateClassificationOfficeProject area
January 31, 2024NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
May 20, 2022NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
June 6, 2018VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
July 18, 2013VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
December 2, 2010NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for Hudson Valley Fertility, PLLC
  • FDA Inspection 1228929 - 2024-01-31
  • FDA Inspection 1170360 - 2022-05-20
  • FDA Inspection 1054546 - 2018-06-06
  • FDA Inspection 840036 - 2013-07-18
  • FDA Inspection 700064 - 2010-12-02

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