FDA inspection

ResMed Ltd.: FDA inspection ending Feb 3, 2011

FDA inspection 714766 · No Action Indicated (NAI) · Bella Vista

Key facts

Inspection ID 714766
Firm ResMed Ltd.
FEI number 3004604967
Address 1 Elizabeth Macarthur Dr
City Bella Vista
Country Australia
Fiscal year 2011
Inspection end date Feb 3, 2011
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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