FDA Inspection 1015921 — Midwest Fertility Specialists

Midwest Fertility Specialists — FEI 3005620323

The FDA completed an inspection of Midwest Fertility Specialists on Jun 21, 2017 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 21, 2017
Fiscal Year
2017
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.