FDA inspection

Zhongshan Transtek Electronics Co., Ltd.: FDA inspection ending Oct 17, 2013

FDA inspection 854360 · Voluntary Action Indicated (VAI) · Zhongshan

Key facts

Inspection ID 854360
Firm Zhongshan Transtek Electronics Co., Ltd.
FEI number 3008485370
Address No. 23 Jin'An Road, Minzhong
City Zhongshan
Country China
Fiscal year 2014
Inspection end date Oct 17, 2013
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 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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