FDA Inspection 1287330 — Huons Co., Ltd.

Huons Co., Ltd. — FEI 3007163376

The FDA completed an inspection of Huons Co., Ltd. on Dec 3, 2025 in Jecheon. 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
Dec 3, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Jecheon (Korea (the Republic of))

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