FDA Inspection
Hudson Valley Fertility, PLLCHudson Valley Fertility, PLLC – FDA Inspection, Jul 18, 2013
Record Details
This FDA Inspection record concerns Hudson Valley Fertility, PLLC, with an inspection on July 18, 2013, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- July 18, 2013
- Product Type
- Biologics
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ID · 8fb8008c-a2cc-4c2a-a9ee-8cd63b629eb4
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 840036
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
FDA Citations
4- 21 CFR 1271.47(d)Departures: recording and justifying
- 21 CFR 1271.55(d)(2)Accurate, indelible, legible
- 21 CFR 1271.47(a)Testing, screening, donor eligibility procedures
- 21 CFR 1271.55(c)Name and personal info on accompanying records
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Hudson Valley Fertility, PLLC
5| Date | Classification | Office | Project area |
|---|---|---|---|
| January 31, 2024 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| May 20, 2022 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| June 6, 2018 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| August 19, 2016 | VAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| December 2, 2010 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for Hudson Valley Fertility, PLLC
- FDA Inspection 1228929 - 2024-01-31
- FDA Inspection 1170360 - 2022-05-20
- FDA Inspection 1054546 - 2018-06-06
- FDA Inspection 985373 - 2016-08-19
- FDA Inspection 700064 - 2010-12-02
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