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FDA Inspection 970173 — Midwest Women's Healthcare Specialists

Midwest Women's Healthcare Specialists — FEI 3006404428

The FDA completed an inspection of Midwest Women's Healthcare Specialists on May 13, 2016 in Kansas City, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 13, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Kansas City, MO (United States)

Facility

Other inspections at this facility

  • 1027697 (NAI Mon Sep 25 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 894605 (NAI Tue Sep 09 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 753495 (NAI Mon Nov 21 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 641105 (VAI Wed Jan 27 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources