FDA Inspection
Offices for Fertility and Reproductive Medicine, P. C.Offices for Fertility and Reproductive Medicine, P. C. – FDA Inspection, Sep 28, 2009
Record Details
This FDA Inspection record concerns Offices for Fertility and Reproductive Medicine, P. C., with an inspection on September 28, 2009, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- September 28, 2009
- Product Type
- Biologics
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ID · 7d29321a-f2c9-408b-a880-679f0ceadc1f
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 615020
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
FDA Citations
3- 21 CFR 1271.55(d)(2)Accurate, indelible, legible
- 21 CFR 1271.47(a)Procedures for all other requirements
- 21 CFR 1271.50(a)Responsible person to determine, document
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Other FDA inspections of Offices for Fertility and Reproductive Medicine, P. C.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| January 31, 2018 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| March 18, 2016 | VAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| May 12, 2014 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| September 25, 2012 | VAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for Offices for Fertility and Reproductive Medicine, P. C.
- FDA Inspection 1039314 - 2018-01-31
- FDA Inspection 962764 - 2016-03-18
- FDA Inspection 878286 - 2014-05-12
- FDA Inspection 800591 - 2012-09-25
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