FDA Inspection 1261763 — EMG Technology Co., Ltd.

EMG Technology Co., Ltd. — FEI 3003803075

The FDA completed an inspection of EMG Technology Co., Ltd. on December 13, 2024 in Taichung City. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 13, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Taichung City (Taiwan)