FDA inspection

Ilion Medical, Inc.: FDA inspection ending Jul 16, 2025

FDA inspection 1276194 · No Action Indicated (NAI) · Minneapolis, MN

Key facts

Inspection ID 1276194
Firm Ilion Medical, Inc.
FEI number 3014919610
Address 825 Nicollet Mall Ste 700
City Minneapolis
State MN
ZIP 55402
Country United States
Fiscal year 2025
Inspection end date Jul 16, 2025
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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