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FDA Inspection
•Resmed Corporation•February 23, 2009

Resmed Corporation – FDA Inspection, Feb 23, 2009

Record Details

This FDA Inspection record concerns Resmed Corporation, with an inspection on February 23, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company
Resmed Corporation
Inspection Date
February 23, 2009
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 63473c4f-8854-4925-8981-083a9017bf39

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
564987
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Resmed Corporation

2
DateClassificationOfficeProject area
December 7, 2016Not classifiedLos Angeles District Office
August 6, 2014NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for Resmed Corporation
  • FDA Inspection 1004697 - 2016-12-07
  • FDA Inspection 890655 - 2014-08-06

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