# FDA Inspection 667581 - Philips Respironics, Inc. - July 01, 2010

Source: https://www.keypedia.com/records/fda_inspections/philips-respironics-inc/933f79ea-aa6c-486f-b1e4-9e25925b828d
Source feed: FDA_Inspections

> FDA Inspection 667581 for Philips Respironics, Inc. on July 01, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 667581
- Company Name: Philips Respironics, Inc.
- Inspection Date: 2010-07-01
- Classification: Voluntary Action Indicated (VAI)
- 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