# FDA Inspection 846118 - Resmed Motor Technologies - August 22, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/resmed-motor-technologies/ff0fb8b7-1a86-46af-a8ec-93dc3dd04e4f/
Source feed: FDA_Inspections

> FDA Inspection 846118 for Resmed Motor Technologies on August 22, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 846118
- Company Name: Resmed Motor Technologies
- Inspection Date: 2013-08-22
- 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 1004519 - 2017-02-16](https://www.globalkeysolutions.net/api/records/fda_inspections/resmed-motor-technologies/273b57a7-6583-43e2-90f1-72b1e90fa0ad/)
- [FDA Inspection 846118 - 2013-08-22](https://www.globalkeysolutions.net/api/records/fda_inspections/resmed-motor-technologies/ed6d9adc-d43a-4384-9c13-9e52016ddfec/)

Company: https://www.globalkeysolutions.net/companies/resmed-motor-technologies/4ccc618a-9ba8-4853-8980-3152f75ec585

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