FDA Inspection 806445 — Midwest Fertility Specialists

Midwest Fertility Specialists — FEI 3005620268

The FDA completed an inspection of Midwest Fertility Specialists on Nov 6, 2012 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
Nov 6, 2012
Fiscal Year
2013
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Fort Wayne, IN (United States)

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