FDA Inspection 1334946 — RADISEN CO. LTD

RADISEN CO. LTD — FEI 3017004860

The FDA completed an inspection of RADISEN CO. LTD on Aug 4, 2026 in Anyang. 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
Aug 4, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Anyang (Korea (the Republic of))