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FDA Inspection 1015921 — Midwest Fertility Specialists

Midwest Fertility Specialists — FEI 3005620323

The FDA completed an inspection of Midwest Fertility Specialists on June 21, 2017 in Carmel, IN. 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
June 21, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Carmel, IN (United States)

Facility

Other inspections at this facility

  • 1255000 (VAI Mon Nov 25 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1109705 (NAI Wed Oct 16 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 931253 (NAI Thu Jun 18 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 816819 (VAI Thu Jan 31 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 660527 (NAI Mon Apr 19 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources