FDA Inspection
Midwest Fertility Center, Corp.Midwest Fertility Center, Corp. – FDA Inspection, Apr 1, 2013
Record Details
This FDA Inspection record concerns Midwest Fertility Center, Corp., with an inspection on April 1, 2013, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- April 1, 2013
- Product Type
- Biologics
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ID · eaa0cb4c-ad50-43d4-81eb-6084d6942287
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 825407
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
FDA Citations
1- 21 CFR 1271.47(a)Testing, screening, donor eligibility procedures
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Other FDA inspections of Midwest Fertility Center, Corp.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| June 28, 2017 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| July 22, 2015 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| June 1, 2011 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for Midwest Fertility Center, Corp.
- FDA Inspection 1017981 - 2017-06-28
- FDA Inspection 935341 - 2015-07-22
- FDA Inspection 727593 - 2011-06-01
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