# Philips North America LLC – FDA Inspection, Mar 19, 2012

Source: https://www.keypedia.com/records/fda_inspections/philips-north-america-llc/34868662-d263-4ea9-9857-3cb3be59124f
Source feed: FDA_Inspections

> FDA inspection 772990 of Philips North America LLC, March 19, 2012. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 812. 12 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 772990
- Company Name: Philips North America LLC
- Inspection Date: 2012-03-19
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

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Company: https://www.keypedia.com/companies/philips-north-america-llc/d7335702-bc34-4fb8-acdc-db91e81d2f8c

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