FDA Inspection
Midwest Women's Healthcare SpecialistsMidwest Women's Healthcare Specialists – FDA Inspection, Jan 27, 2010
Record Details
This FDA Inspection record concerns Midwest Women's Healthcare Specialists, with an inspection on January 27, 2010, issued by the Center for Biologics Evaluation and Research, covering biologics.
- Inspection Date
- January 27, 2010
- Product Type
- Biologics
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ID · 2fe671cf-43fc-4775-9019-7d289ee8c2fd
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 641105
- FDA center
- Biologics
- Project area
- Human Cellular, Tissue, and Gene Therapies
FDA Citations
2- 21 CFR 1271.47(a)Testing, screening, donor eligibility procedures
- 21 CFR 1271.150(c)(1)(iii)Ensurane of compliance
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Other FDA inspections of Midwest Women's Healthcare Specialists
4| Date | Classification | Office | Project area |
|---|---|---|---|
| September 25, 2017 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| May 13, 2016 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| September 9, 2014 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
| November 21, 2011 | NAI | Center for Biologics Evaluation and Research | Human Cellular, Tissue, and Gene Therapies |
Other documents for Midwest Women's Healthcare Specialists
- FDA Inspection 1027697 - 2017-09-25
- FDA Inspection 970173 - 2016-05-13
- FDA Inspection 894605 - 2014-09-09
- FDA Inspection 753495 - 2011-11-21
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