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FDA Inspection
•Caperton Fertility Institute LLC•October 17, 2017

Caperton Fertility Institute LLC – FDA Inspection, Oct 17, 2017

Record Details

This FDA Inspection record concerns Caperton Fertility Institute LLC, with an inspection on October 17, 2017, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Caperton Fertility Institute LLC
Inspection Date
October 17, 2017
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Gloria A. Milster (FDA Associated Person)
View Company Profile

ID · 860591de-f85c-4a3f-8eb2-7230ccefe0d3

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1029179
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 1271.47(a)Testing, screening, donor eligibility procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Caperton Fertility Institute LLC

2
DateClassificationOfficeProject area
September 18, 2025Not classifiedDenver District Office
September 18, 2020NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
Other documents for Caperton Fertility Institute LLC
  • FDA Inspection 1287272 - 2025-09-18
  • FDA Inspection 1130278 - 2020-09-18

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