FDA inspection

Beijing Syntech Laser Co., Ltd: FDA inspection ending Jul 12, 2013

FDA inspection 841544 · Voluntary Action Indicated (VAI) · Beijing

Key facts

Inspection ID 841544
Firm Beijing Syntech Laser Co., Ltd
FEI number 3007535734
Address International Industry Base, F/4; No. 8 Liye Road; West Area Changping
City Beijing
Country China
Fiscal year 2013
Inspection end date Jul 12, 2013
Classification Voluntary Action Indicated (VAI)
Project area Compliance: 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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