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FDA Inspection
•California Center for Reproductive Health•July 15, 2024

California Center for Reproductive Health – FDA Inspection, Jul 15, 2024

Record Details

This FDA Inspection record concerns California Center for Reproductive Health, with an inspection on July 15, 2024, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
California Center for Reproductive Health
Inspection Date
July 15, 2024
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Dylan R. Jock (Issuing Officer)
View Company Profile

ID · 92b012be-1d4b-46ff-827d-ab0a87e91253

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1243852
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

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 California Center for Reproductive Health

4
DateClassificationOfficeProject area
August 9, 2023Not classifiedLos Angeles District Office
July 12, 2018VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
June 7, 2016NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
February 17, 2012NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for California Center for Reproductive Health
  • FDA Inspection 1214495 - 2023-08-09
  • FDA Inspection 1058641 - 2018-07-12
  • FDA Inspection 972639 - 2016-06-07
  • FDA Inspection 769379 - 2012-02-17

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