FDA inspection

Everlife Medical Equipment Co., Ltd.: FDA inspection ending Dec 14, 2017

FDA inspection 1037883 · Voluntary Action Indicated (VAI) · New Taipei City

Key facts

Inspection ID 1037883
Firm Everlife Medical Equipment Co., Ltd.
FEI number 3004753827
Address Bao-Qiao Road, Xin-Dian District, 8th Floor; No. 8 Lane 235
City New Taipei City
Country Taiwan
Fiscal year 2018
Inspection end date Dec 14, 2017
Classification Voluntary Action Indicated (VAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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