FDA Inspection 1079196 — GALEMED CORP.

GALEMED CORP. — FEI 3003319165

The FDA completed an inspection of GALEMED CORP. on December 6, 2018 in Wu-Jia. 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 6, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Wu-Jia (Taiwan)