FDA Inspection 931253 — Midwest Fertility Specialists

Midwest Fertility Specialists — FEI 3005620323

The FDA completed an inspection of Midwest Fertility Specialists on Jun 18, 2015 in Carmel, 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
Jun 18, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Carmel, IN (United States)

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