# FDA Inspection 872982 - ResMed Ltd. - February 13, 2014

Source: https://www.keypedia.com/records/fda_inspections/resmed-ltd/8180fc04-342b-4e9d-a5e1-24e5fe3226c9
Source feed: FDA_Inspections

> FDA Inspection 872982 for ResMed Ltd. on February 13, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 872982
- Company Name: ResMed Ltd.
- Inspection Date: 2014-02-13
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 872982 - 2014-02-13](https://www.keypedia.com/records/fda_inspections/resmed-ltd/fefd799c-270b-4169-b437-8c675757b24f)
- [FDA Inspection 714766 - 2011-02-03](https://www.keypedia.com/records/fda_inspections/resmed-ltd/3adfd9db-0931-439d-975c-392245c870ed)

Company: https://www.keypedia.com/companies/resmed-ltd/11fad8d1-96f0-41e9-8609-2e62ba6b86bd

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7