# FDA Inspection 669123 - Philips Healthcare - June 18, 2010

Source: https://www.keypedia.com/records/fda_inspections/philips-healthcare/f0250772-4ec2-42ae-b4c6-e2b345397a7e
Source feed: FDA_Inspections

> FDA Inspection 669123 for Philips Healthcare on June 18, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 669123
- Company Name: Philips Healthcare
- Inspection Date: 2010-06-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/philips-healthcare/460a2a6d-0a19-4e50-8a72-3fe8d4a47559

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