FDA Inspection 1091287 — Everyway Medical Instruments Co., Inc.

Everyway Medical Instruments Co., Inc. — FEI 3002552319

The FDA completed an inspection of Everyway Medical Instruments Co., Inc. on May 16, 2019 in New Taipei 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
May 16, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
New Taipei City (Taiwan)