# FDA Inspection 607750 - Philips North America - July 18, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/philips-north-america/a332af6f-3b1e-4acf-a072-6780f99f7a32
Source feed: FDA_Inspections

> FDA Inspection 607750 for Philips North America on July 18, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 607750
- Company Name: Philips North America
- Inspection Date: 2009-07-18
- Classification: Voluntary Action Indicated (VAI)
- 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/62465dd7-c599-42c6-bd2e-5794bc5f4de2

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