FDA Inspection
Center for Reproductive Medicine of New MexicoCenter for Reproductive Medicine of New Mexico – FDA Inspection, Feb 5, 2016
Record Details
This FDA Inspection record concerns Center for Reproductive Medicine of New Mexico, with an inspection on February 5, 2016, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- February 5, 2016
- Product Type
- Biologics
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ID · 95ae44bd-a695-4d6d-b219-d8eec1bb7238
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 980251
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
FDA Citations
1- 21 CFR 1271.50(a)Responsible person to determine, document
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Other FDA inspections of Center for Reproductive Medicine of New Mexico
3| Date | Classification | Office | Project area |
|---|---|---|---|
| July 26, 2011 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| March 7, 2011 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| January 27, 2009 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for Center for Reproductive Medicine of New Mexico
- FDA Inspection 749459 - 2011-07-26
- FDA Inspection 714328 - 2011-03-07
- FDA Inspection 565101 - 2009-01-27
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