# FDA Inspection 928472 - Respironics, Inc. DBA Philips Respironics - July 21, 2014

Source: https://www.keypedia.com/records/fda_inspections/respironics-inc-dba-philips-respironics/8e623626-d965-4cbd-b214-af2feda2c8e1
Source feed: FDA_Inspections

> FDA Inspection 928472 for Respironics, Inc. DBA Philips Respironics on July 21, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 928472
- Company Name: Respironics, Inc. DBA Philips Respironics
- Inspection Date: 2014-07-21
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 928472 - 2014-07-21](https://www.keypedia.com/records/fda_inspections/respironics-inc-dba-philips-respironics/4a4073c7-e475-4e72-9498-1ecdd548918b)
- [FDA Inspection 794374 - 2012-07-31](https://www.keypedia.com/records/fda_inspections/respironics-inc-dba-philips-respironics/9897934d-6b23-4874-8845-59aadadc7cfe)
- [FDA Inspection 794374 - 2012-07-31](https://www.keypedia.com/records/fda_inspections/respironics-inc-dba-philips-respironics/0a90ed44-ee8f-4849-8e25-236b2a934c7a)
- [FDA Inspection 610289 - 2009-09-04](https://www.keypedia.com/records/fda_inspections/respironics-inc-dba-philips-respironics/356939a8-a93b-4394-ac82-68ab475a672f)
- [FDA Inspection 610289 - 2009-09-04](https://www.keypedia.com/records/fda_inspections/respironics-inc-dba-philips-respironics/7fff2430-1084-4071-aa16-5ec164e9d0f9)

Company: https://www.keypedia.com/companies/respironics-inc-dba-philips-respironics/d8574fe7-d9ee-4bd3-a298-c0d2b0c045f6

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