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483
•Women & Infants Hospital Of Rhode Island Women & Infants' Fertility Center•January 27, 2020

Women & Infants Hospital Of Rhode Island Women & Infants' Fertility Center – FDA 483, Jan 27, 2020

Record Details

Women & Infants Hospital Of Rhode Island, a human reproductive establishment, received a Form 483 citing two observations related to donor screening. The facility failed to adequately screen an oocyte donor for Zika virus risk factors due to an incomplete medical history form. Additionally, the firm lacked established written procedures for HCT/P donor screening, specifically for medical health history interviews.

Company
Women & Infants Hospital Of Rhode Island Women & Infants' Fertility Center
Inspection date
January 27, 2020
Product type
biologics
Office
Division of Northeast Imports 
Person
  • Lorayne A McGuinness
View Company Profile

ID · 418facbf-9028-4e9f-9d1a-9fc7bb1fbcb7

Other documents for Women & Infants Hospital Of Rhode Island Women & Infants' Fertility Center
  • 483 - 2021-08-10August 10, 2021

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