# Philips Respironics, Inc. – FDA Inspection, Jun 24, 2011

Source: https://www.keypedia.com/records/fda_inspections/philips-respironics-inc/9c755046-b873-4021-b727-b32f8ae8e8a1
Source feed: FDA_Inspections

> FDA inspection 733052 of Philips Respironics, Inc., June 24, 2011. Classification: Official Action Indicated (OAI). 2 citations under 21 CFR parts 803 and 820. 16 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 733052
- Company Name: Philips Respironics, Inc.
- Inspection Date: 2011-06-24
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

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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