FDA Inspection
Assisted Reproductive Technologies Medical Group IncAssisted Reproductive Technologies Medical Group Inc – FDA Inspection, Aug 3, 2011
Record Details
This FDA Inspection record concerns Assisted Reproductive Technologies Medical Group Inc, with an inspection on August 3, 2011, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- August 3, 2011
- Product Type
- Biologics
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ID · 8477b02a-7aa5-4019-9ba7-e225f223eb11
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 739235
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
FDA Citations
1- 21 CFR 1271.80(d)(1)Reactive tests--not determined ineligible
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Other FDA inspections of Assisted Reproductive Technologies Medical Group Inc
4| Date | Classification | Office | Project area |
|---|---|---|---|
| May 27, 2026 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| March 20, 2023 | NAI | Center for Biologics Evaluation and Research | Vaccines and Allergenic Products |
| June 29, 2018 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| February 29, 2016 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for Assisted Reproductive Technologies Medical Group Inc
- FDA Inspection 1320230 - 2026-05-27
- FDA Inspection 1200418 - 2023-03-20
- FDA Inspection 1060618 - 2018-06-29
- FDA Inspection 960529 - 2016-02-29
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