FDA Inspection
Midwest Reproductive Center PAMidwest Reproductive Center PA – FDA Inspection, Mar 31, 2011
Record Details
This FDA Inspection record concerns Midwest Reproductive Center PA, with an inspection on March 31, 2011, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- March 31, 2011
- Product Type
- Biologics
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ID · d5c8b88e-77be-4943-a53d-772db6010dc8
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 715696
- 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 Reproductive Center PA
5| Date | Classification | Office | Project area |
|---|---|---|---|
| April 22, 2025 | Not classified | Kansas City District Office | |
| March 9, 2020 | NAI | Center for Biologics Evaluation and Research | Vaccines and Allergenic Products |
| April 24, 2018 | NAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| October 9, 2015 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| September 11, 2014 | VAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for Midwest Reproductive Center PA
- FDA Inspection 1269881 - 2025-04-22
- FDA Inspection 1121458 - 2020-03-09
- FDA Inspection 1049734 - 2018-04-24
- FDA Inspection 945978 - 2015-10-09
- FDA Inspection 895039 - 2014-09-11
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