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483
•Montefiore's Institute for Reproductive Medicine and Health•May 3, 2019

Montefiore's Institute for Reproductive Medicine and Health – FDA 483, May 3, 2019

Record Details

An FDA inspection of Montefiore's Institute for Reproductive Medicine and Health in Hartsdale, NY, revealed two significant observations related to human reproductive tissue. The firm failed to properly determine and document the eligibility of oocyte donors, specifically by not testing for West Nile Virus. Additionally, the firm's standard operating procedures for egg donor screening were not revised to include seasonal West Nile Virus testing.

Company
Montefiore's Institute for Reproductive Medicine and Health
Inspection date
May 3, 2019
Product type
biologics
Office
Division of Human and Animal Food Operations - East I
Person
  • Anthony N. Onianwa (Investigator)
View Company Profile

ID · 8ec76984-a358-47fb-a632-f8ae5e62b858

Other documents for Montefiore's Institute for Reproductive Medicine and Health
  • 483 - 2021-08-16August 16, 2021

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