FDA Inspection 1091287 — Everyway Medical Instruments Co., Ltd

Everyway Medical Instruments Co., Ltd — FEI 3002552319

The FDA completed an inspection of Everyway Medical Instruments Co., Ltd on May 16, 2019 in New Taipei City. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
May 16, 2019
Fiscal Year
2019
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.