FDA Inspection 1020815 — Midwest Fertility Specialists

Midwest Fertility Specialists — FEI 3005620268

The FDA completed an inspection of Midwest Fertility Specialists on Aug 1, 2017 in Fort Wayne, IN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Aug 1, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Fort Wayne, IN (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.