FDA Inspection 919408 — Midwest Fertility Specialists

Midwest Fertility Specialists — FEI 3005620268

The FDA completed an inspection of Midwest Fertility Specialists on March 25, 2015 in Fort Wayne, 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
March 25, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Fort Wayne, IN (United States)