FDA inspection

JIANGSU WEIKANG JIEJING MEDICAL APPARATUS CO., LTD.: FDA inspection ending Apr 27, 2016

FDA inspection 985995 · No Action Indicated (NAI) · Shuyang

Key facts

Inspection ID 985995
Firm JIANGSU WEIKANG JIEJING MEDICAL APPARATUS CO., LTD.
FEI number 3010594263
Address # 18 Wenzhou Road, Economical Development District
City Shuyang
Country China
Fiscal year 2016
Inspection end date Apr 27, 2016
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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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