# FDA Inspection 569821 - Philips North  America, LLC - March 10, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/philips-north-america-llc/de9ee8ca-f41d-432c-bb13-46b2d7ab66e6
Source feed: FDA_Inspections

> FDA Inspection 569821 for Philips North  America, LLC on March 10, 2009. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 569821
- Company Name: Philips North  America, LLC
- Inspection Date: 2009-03-10
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/philips-north-america-llc/79612d5c-f4a6-4cc1-8134-f23502db5bf9

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