# FDA Inspection 666831 - Philips Respironics, Inc. - May 26, 2010

Source: https://www.keypedia.com/records/fda_inspections/philips-respironics-inc/15f34c07-4aab-43cf-a2c3-2f1ffa56cb1f
Source feed: FDA_Inspections

> FDA Inspection 666831 for Philips Respironics, Inc. on May 26, 2010. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 666831
- Company Name: Philips Respironics, Inc.
- Inspection Date: 2010-05-26
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/philips-respironics-inc/03ceee46-7a72-4590-8bc4-8033e1503cf3

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