# Philips Burton – FDA Inspection, Nov 10, 2011

Source: https://www.keypedia.com/records/fda_inspections/philips-burton/7faa4923-0467-4d63-8848-f246b6973c66
Source feed: FDA_Inspections

> FDA inspection 753037 of Philips Burton, November 10, 2011. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 753037
- Company Name: Philips Burton
- Inspection Date: 2011-11-10
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

Company: https://www.keypedia.com/companies/philips-burton/76c4af3a-3780-4efc-b6f9-f6c8bd584d1a

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