FDA inspection

Changzhou Orthmed Medical Instrument Co., Ltd.: FDA inspection ending May 30, 2013

FDA inspection 838678 · Voluntary Action Indicated (VAI) · Changzhou

Key facts

Inspection ID 838678
Firm Changzhou Orthmed Medical Instrument Co., Ltd.
FEI number 3005596372
Address NO. 177 Qinlinglu, Xinbei
City Changzhou
Country China
Fiscal year 2013
Inspection end date May 30, 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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