# FDA Inspection 890655 - Resmed Corporation - August 06, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/resmed-corporation/fa4ce225-7571-41cd-a598-043c02944323/
Source feed: FDA_Inspections

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

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## Details

- Record Type: FDA Inspection
- Inspection ID: 890655
- Company Name: Resmed Corporation
- Inspection Date: 2014-08-06
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 890655 - 2014-08-06](https://www.globalkeysolutions.net/api/records/fda_inspections/resmed-corporation/93763741-f0d1-4a75-86fb-4f3f466cb539/)
- [FDA Inspection 564987 - 2009-02-23](https://www.globalkeysolutions.net/api/records/fda_inspections/resmed-corporation/63473c4f-8854-4925-8981-083a9017bf39/)
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Company: https://www.globalkeysolutions.net/companies/resmed-corporation/c7be6be5-c615-4efc-8478-2df25b59cc93

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