FDA Inspection 1276194 — Ilion Medical, Inc.

Ilion Medical, Inc. — FEI 3014919610

The FDA completed an inspection of Ilion Medical, Inc. on Jul 16, 2025 in Minneapolis, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 16, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Minneapolis, MN (United States)

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