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FDA Inspection
•Westchester IVF•March 29, 2019

Westchester IVF – FDA Inspection, Mar 29, 2019

Record Details

This FDA Inspection record concerns Westchester IVF, with an inspection on March 29, 2019, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Westchester IVF
Inspection Date
March 29, 2019
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Anthony N. Onianwa (FDA Associated Person)
View Company Profile

ID · f9e20a62-ac98-4552-bfcb-b9763bebfa66

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1085714
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

Other FDA inspections of Westchester IVF

6
DateClassificationOfficeProject area
March 9, 2026NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
October 27, 2022NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
September 12, 2016NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
February 19, 2015VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
June 12, 2013VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
View all 6 other inspections on the company page
Other documents for Westchester IVF
  • FDA Inspection 1310364 - 2026-03-09
  • FDA Inspection 1183798 - 2022-10-27
  • FDA Inspection 984424 - 2016-09-12
  • FDA Inspection 918290 - 2015-02-19
  • FDA Inspection 838589 - 2013-06-12

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