# FDA Inspection 551807 - PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. - November 20, 2008

Source: https://www.keypedia.com/records/fda_inspections/philips-medical-systems-nederland-bv/830f6365-0a3b-43fe-bb46-18dbf11367a3
Source feed: FDA_Inspections

> FDA Inspection 551807 for PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. on November 20, 2008. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 551807
- Company Name: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Inspection Date: 2008-11-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/philips-medical-systems-nederland-bv/667b13ad-6e74-4448-9805-0b13c8c26e46

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