FDA inspection

ResMed Ltd.: FDA inspection ending Feb 13, 2014

FDA inspection 872982 · No Action Indicated (NAI) · Bella Vista

Key facts

Inspection ID 872982
Firm ResMed Ltd.
FEI number 3004604967
Address 1 Elizabeth Macarthur Dr
City Bella Vista
Country Australia
Fiscal year 2014
Inspection end date Feb 13, 2014
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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