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FDA Inspection
•West Coast Fertility Centers, LLC•June 5, 2023

West Coast Fertility Centers, LLC – FDA Inspection, Jun 5, 2023

Record Details

This FDA Inspection record concerns West Coast Fertility Centers, LLC, with an inspection on June 5, 2023, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
West Coast Fertility Centers, LLC
Inspection Date
June 5, 2023
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Creighton T. Tuzon (Issuing Officer)
View Company Profile

ID · eb958ed5-19b1-4989-a1bc-916534321e45

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1207134
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 1271.47(a)Testing, screening, donor eligibility procedures
  2. 21 CFR 1271.75(a)(1)Risk factors, clinical evidence

Full citation text and observation details available on the Dashboard.

Other FDA inspections of West Coast Fertility Centers, LLC

4
DateClassificationOfficeProject area
April 15, 2025Not classifiedLos Angeles District Office
December 27, 2017VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 26, 2016NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
February 24, 2012VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for West Coast Fertility Centers, LLC
  • FDA Inspection 1267741 - 2025-04-15
  • FDA Inspection 1036342 - 2017-12-27
  • FDA Inspection 963395 - 2016-02-26
  • FDA Inspection 770190 - 2012-02-24

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