FDA Inspection
Foulk & Whitten Nevada Center For Reproductive MedicineFoulk & Whitten Nevada Center For Reproductive Medicine – FDA Inspection, Nov 16, 2016
Record Details
This FDA Inspection record concerns Foulk & Whitten Nevada Center For Reproductive Medicine, with an inspection on November 16, 2016, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- November 16, 2016
- Product Type
- Biologics
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ID · 517b4154-d30a-4cd4-aec9-9f698794948c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 993202
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 1271.65(b)(2)Labeled re: biohazard, risks, test results
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Other FDA inspections of Foulk & Whitten Nevada Center For Reproductive Medicine
5| Date | Classification | Office | Project area |
|---|---|---|---|
| November 15, 2023 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| March 28, 2019 | VAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| June 5, 2014 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| May 31, 2011 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| May 6, 2009 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for Foulk & Whitten Nevada Center For Reproductive Medicine
- FDA Inspection 1223875 - 2023-11-15
- FDA Inspection 1084676 - 2019-03-28
- FDA Inspection 883672 - 2014-06-05
- FDA Inspection 727117 - 2011-05-31
- FDA Inspection 583033 - 2009-05-06
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