FDA inspection

Shenzhen Jumper Medical Equipment Co., Ltd.: FDA inspection ending Feb 13, 2015

FDA inspection 914049 · Voluntary Action Indicated (VAI) · Shenzhen

Key facts

Inspection ID 914049
Firm Shenzhen Jumper Medical Equipment Co., Ltd.
FEI number 3008973759
Address D Building, NO. 71 Xintain Road
City Shenzhen
Country China
Fiscal year 2015
Inspection end date Feb 13, 2015
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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