FDA Inspection 890655 - Resmed Corporation - August 06, 2014

FDA Inspection 890655 for Resmed Corporation on August 06, 2014. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 890655 for Resmed Corporation on August 06, 2014. Classification: No Action Indicated (NAI).

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Record Information

Company

Resmed Corporation

Inspection Date

August 6, 2014

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fa4ce225-7571-41cd-a598-043c02944323

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