FDA Inspection
Huntington Reproductive CenterHuntington Reproductive Center – FDA Inspection, Aug 11, 2011
Record Details
This FDA Inspection record concerns Huntington Reproductive Center, with an inspection on August 11, 2011, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- August 11, 2011
- Product Type
- Biologics
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ID · 9c0f4dfb-967d-4437-b268-6433cc8e9d49
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 739237
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
FDA Citations
1- 21 CFR 1271.50(a)Determination based on screening and testing
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Other FDA inspections of Huntington Reproductive Center
5| Date | Classification | Office | Project area |
|---|---|---|---|
| September 15, 2025 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| March 19, 2025 | Not classified | Los Angeles District Office | |
| March 29, 2019 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| February 12, 2014 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| July 9, 2009 | VAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for Huntington Reproductive Center
- FDA Inspection 1293834 - 2025-09-15
- FDA Inspection 1264971 - 2025-03-19
- FDA Inspection 1086929 - 2019-03-29
- FDA Inspection 866901 - 2014-02-12
- FDA Inspection 599961 - 2009-07-09
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