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FDA Inspection
•Texas Center for Reproductive Health•February 12, 2013

Texas Center for Reproductive Health – FDA Inspection, Feb 12, 2013

Record Details

This FDA Inspection record concerns Texas Center for Reproductive Health, with an inspection on February 12, 2013, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Texas Center for Reproductive Health
Inspection Date
February 12, 2013
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
View Company Profile

ID · aed49ed4-825a-4d18-bcc7-d76292b0603a

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
818101
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

FDA Citations

1
  1. 21 CFR 1271.75(a)(1)Risk factors, clinical evidence

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Texas Center for Reproductive Health

4
DateClassificationOfficeProject area
March 6, 2025Not classifiedDallas District Office
November 7, 2018NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
February 4, 2016VAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
May 20, 2010NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for Texas Center for Reproductive Health
  • FDA Inspection 1263527 - 2025-03-06
  • FDA Inspection 1073733 - 2018-11-07
  • FDA Inspection 957609 - 2016-02-04
  • FDA Inspection 665565 - 2010-05-20

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