FDA inspection

Edan Instruments, Inc.: FDA inspection ending Nov 29, 2012

FDA inspection 812416 · No Action Indicated (NAI) · Shenzhen

Key facts

Inspection ID 812416
Firm Edan Instruments, Inc.
FEI number 3003971136
Address Jinsha Comm., 15 Jinhui Road, Pingshan; Longgang
City Shenzhen
Country China
Fiscal year 2013
Inspection end date Nov 29, 2012
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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