FDA inspection

ZHONGSHAN A&J MEDICAL EQUIPMENT CO., LTD. (JBS): FDA inspection ending Jul 20, 2016

FDA inspection 981852 · Voluntary Action Indicated (VAI) · Zhongshan

Key facts

Inspection ID 981852
Firm ZHONGSHAN A&J MEDICAL EQUIPMENT CO., LTD. (JBS)
FEI number 3008555994
Address No 2 Shang Zha Street
City Zhongshan
Country China
Fiscal year 2016
Inspection end date Jul 20, 2016
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: 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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