FDA inspection

SHENZHEN KINGYIELD TECHNOLOGY CO., LTD: FDA inspection ending May 4, 2012

FDA inspection 780529 · Voluntary Action Indicated (VAI) · Shenzhen China

Key facts

Inspection ID 780529
Firm SHENZHEN KINGYIELD TECHNOLOGY CO., LTD
FEI number 3007420856
Address SECTION C1 C2 FU HAI INDUSTRIAL ZONE, FU YONG STREET BAOAN
City Shenzhen China
Country China
Fiscal year 2012
Inspection end date May 4, 2012
Classification Voluntary Action Indicated (VAI)
Project area Compliance: 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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