FDA inspection

Suzhou Dukangning Medical Products Co., Ltd.: FDA inspection ending May 29, 2014

FDA inspection 882587 · Voluntary Action Indicated (VAI) · Suzhou

Key facts

Inspection ID 882587
Firm Suzhou Dukangning Medical Products Co., Ltd.
FEI number 3004967902
Address 22 Wanping West Rd, Hengshanzhen Wujiang
City Suzhou
Country China
Fiscal year 2014
Inspection end date May 29, 2014
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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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