FDA Inspection 1029727 — FreeRider Corporation

FreeRider Corporation — FEI 3003820676

The FDA completed an inspection of FreeRider Corporation on September 21, 2017 in Kaohsiung 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
September 21, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Kaohsiung City (Taiwan)