FDA inspection

Turnxon Precision Co.,Ltd.: FDA inspection ending Jul 12, 2017

FDA inspection 1019289 · Voluntary Action Indicated (VAI) · Dongguan

Key facts

Inspection ID 1019289
Firm Turnxon Precision Co.,Ltd.
FEI number 3011534620
Address Tangjiao Industry Park, Chashan Town
City Dongguan
Country China
Fiscal year 2017
Inspection end date Jul 12, 2017
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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