FDA inspection

ResMed Ltd.: FDA inspection ending Aug 25, 2017

FDA inspection 1034874 · No Action Indicated (NAI) · Bella Vista

Key facts

Inspection ID 1034874
Firm ResMed Ltd.
FEI number 3004604967
Address 1 Elizabeth Macarthur Dr
City Bella Vista
Fiscal year 2017
Inspection end date Aug 25, 2017
Classification No Action Indicated (NAI)
Project area Compliance: Medical Devices
Product type Devices

At a glance

  • None Citations
  • None 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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