# FDA Inspection 891601 - Resmed Germany Inc - July 10, 2014

Source: https://www.keypedia.com/records/fda_inspections/resmed-germany-inc/c591a05f-26a5-4f1f-908f-db613e0331b8
Source feed: FDA_Inspections

> FDA Inspection 891601 for Resmed Germany Inc on July 10, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 891601
- Company Name: Resmed Germany Inc
- Inspection Date: 2014-07-10
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/resmed-germany-inc/e87478c4-6557-4b05-ba33-e4285c0ac752

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