FDA inspection

GVS Technology (Suzhou) Co., Ltd: FDA inspection ending May 21, 2015

FDA inspection 931876 · Voluntary Action Indicated (VAI) · Suzhou

Key facts

Inspection ID 931876
Firm GVS Technology (Suzhou) Co., Ltd
FEI number 3005855942
Address No. 602 Changjiang Road, FegQiao Civil-Run Scitech Park
City Suzhou
Country China
Fiscal year 2015
Inspection end date May 21, 2015
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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