FDA Inspection
Houston Assisted Reproductive Technologies, PLLCHouston Assisted Reproductive Technologies, PLLC – FDA Inspection, Oct 23, 2017
Record Details
This FDA Inspection record concerns Houston Assisted Reproductive Technologies, PLLC, with an inspection on October 23, 2017, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- October 23, 2017
- Product Type
- Biologics
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ID · e4a41112-2f40-4e02-a776-025bd074cffe
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1029763
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
- Outcome
- Form 483 issued
FDA Citations
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 Houston Assisted Reproductive Technologies, PLLC
4| Date | Classification | Office | Project area |
|---|---|---|---|
| August 7, 2026 | Not classified | Dallas District Office | Human Cellular, Tissue, and Gene Therapies |
| February 9, 2022 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| September 29, 2014 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| October 27, 2011 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for Houston Assisted Reproductive Technologies, PLLC
- FDA Inspection 1329880 - 2026-08-07
- FDA Inspection 1162284 - 2022-02-09
- FDA Inspection 898330 - 2014-09-29
- FDA Inspection 751556 - 2011-10-27
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