# Philips Electronics North America Corporation – FDA Inspection, Aug 31, 2017

Source: https://www.keypedia.com/records/fda_inspections/philips-electronics-north-america-corporation/d19a8b7e-1f44-4797-be5d-23749eb13383
Source feed: FDA_Inspections

> FDA inspection 1023742 of Philips Electronics North America Corporation, August 31, 2017. Classification: Voluntary Action Indicated (VAI). Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1023742
- Company Name: Philips Electronics North America Corporation
- Inspection Date: 2017-08-31
- 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: 0

## Related Documents

- FDA Inspection 806265 - 2012-10-30

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/edward-e-lockwood/3260b39e-9211-489f-8247-0ec3353e57ca)

Company: https://www.keypedia.com/companies/philips-electronics-north-america-corporation/6b6a3065-ebd6-47df-86a7-ced067e5bb9d

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