FDA Inspection
Foulk Nevada Fertility Center, PCFoulk Nevada Fertility Center, PC – FDA Inspection, Jan 31, 2020
Record Details
This FDA Inspection record concerns Foulk Nevada Fertility Center, PC, with an inspection on January 31, 2020, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- January 31, 2020
- Product Type
- Biologics
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ID · cb56c4bc-ab10-4c34-9dcf-2c677b667149
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1116752
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
FDA Citations
3- 21 CFR 1271.55(d)(2)Accurate, indelible, legible
- 21 CFR 1271.75(a)(1)Risk factors, clinical evidence
- 21 CFR 1271.47(a)Testing, screening, donor eligibility procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Foulk Nevada Fertility Center, PC
8| Date | Classification | Office | Project area |
|---|---|---|---|
| April 11, 2024 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| February 8, 2019 | VAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| February 1, 2018 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| May 19, 2016 | VAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| June 25, 2013 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for Foulk Nevada Fertility Center, PC
- FDA Inspection 1236180 - 2024-04-11
- FDA Inspection 1078892 - 2019-02-08
- FDA Inspection 1040654 - 2018-02-01
- FDA Inspection 970558 - 2016-05-19
- FDA Inspection 838595 - 2013-06-25
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