FDA Inspection 1274248 — DARI Motion, Inc.

DARI Motion, Inc. — FEI 3015443141

The FDA completed an inspection of DARI Motion, Inc. on June 24, 2025 in Overland Park, KS. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 24, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Overland Park, KS (United States)