FDA Inspection 1335888 — Everyway Medical Instruments Co., Ltd

Everyway Medical Instruments Co., Ltd — FEI 3002552319

The FDA completed an inspection of Everyway Medical Instruments Co., Ltd on Aug 12, 2026 in New Taipei City. 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
Aug 12, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
New Taipei City (Taiwan)

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