FDA Inspection 709033 — Everyway Medical Instruments Co., Ltd

Everyway Medical Instruments Co., Ltd — FEI 3002552319

The FDA completed an inspection of Everyway Medical Instruments Co., Ltd on Jan 20, 2011 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
Jan 20, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
New Taipei City (Taiwan)

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