# Resmed Corporation – FDA Inspection, Aug 6, 2014

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

> FDA inspection 890655 of Resmed Corporation, August 06, 2014. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 890655
- Company Name: Resmed Corporation
- Inspection Date: 2014-08-06
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1004697 - 2016-12-07
- [FDA Inspection 564987 - 2009-02-23](https://www.keypedia.com/records/fda_inspections/resmed-corporation/63473c4f-8854-4925-8981-083a9017bf39)

Company: https://www.keypedia.com/companies/resmed-corporation/c7be6be5-c615-4efc-8478-2df25b59cc93

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