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FDA Inspection
•Brown Fertility Associates, PA•November 9, 2017

Brown Fertility Associates, PA – FDA Inspection, Nov 9, 2017

Record Details

This FDA Inspection record concerns Brown Fertility Associates, PA, with an inspection on November 9, 2017, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Brown Fertility Associates, PA
Inspection Date
November 9, 2017
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Valerie J. Grecek-Trinh (Issuing Officer)
View Company Profile

ID · 1711eaa2-a004-4966-be01-14ef420a889b

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1031252
FDA center
Biologics
Project area
Blood and Blood Products
Outcome
Form 483 issued

Other FDA inspections of Brown Fertility Associates, PA

5
DateClassificationOfficeProject area
October 15, 2025NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
September 25, 2024VAIFlorida District OfficeHuman Cellular, Tissue, and Gene Therapies
January 9, 2020VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
October 29, 2015VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
January 28, 2013VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for Brown Fertility Associates, PA
  • FDA Inspection 1288928 - 2025-10-15
  • FDA Inspection 1250057 - 2024-09-25
  • FDA Inspection 1114658 - 2020-01-09
  • FDA Inspection 947767 - 2015-10-29
  • FDA Inspection 814880 - 2013-01-28

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