# Philips North America LLC – FDA Inspection, Aug 29, 2012

Source: https://www.keypedia.com/records/fda_inspections/philips-north-america-llc/d62da4b7-87a3-4073-a906-7943704db483
Source feed: FDA_Inspections

> FDA inspection 801680 of Philips North America LLC, August 29, 2012. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 12 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 801680
- Company Name: Philips North America LLC
- Inspection Date: 2012-08-29
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

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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