# Philips North America – FDA Inspection, Mar 3, 2017

Source: https://www.keypedia.com/records/fda_inspections/philips-north-america/e2cb00cf-409d-4f2c-b923-99f98a7a6b0a
Source feed: FDA_Inspections

> FDA inspection 1005211 of Philips North America, March 03, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1005211
- Company Name: Philips North America
- Inspection Date: 2017-03-03
- 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: 2

## Related Documents

- [FDA Inspection 1224855 - 2023-12-13](https://www.keypedia.com/records/fda_inspections/philips-north-america/c904f90c-ace0-49c7-b3f3-d5212e6e6fdb)
- [FDA Inspection 777361 - 2012-04-13](https://www.keypedia.com/records/fda_inspections/philips-north-america/30d66b08-2cf6-4bf5-9820-18c0c8f31609)
- FDA Inspection 607750 - 2009-07-18

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/stephen-c-smith/426649fa-0e5b-4b35-ba41-636512a06a48)

Company: https://www.keypedia.com/companies/philips-north-america/62465dd7-c599-42c6-bd2e-5794bc5f4de2

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