# Philips North America LLC – FDA Inspection, Dec 3, 2018

Source: https://www.keypedia.com/records/fda_inspections/philips-north-america-llc/fd06173c-a691-4681-bd6d-ce4d541fb130
Source feed: FDA_Inspections

> FDA inspection 1073302 of Philips North America LLC, December 03, 2018. Classification: Official Action Indicated (OAI). Form 483 issued. 12 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1073302
- Company Name: Philips North America LLC
- Inspection Date: 2018-12-03
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

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## Related Officers

- [Company Rep](https://www.keypedia.com/people/paul-m-kawamoto/0a24b110-12de-4736-8d98-7a023ceec01e)
- [FDA Associated Person](https://www.keypedia.com/people/phillip-m-pontikos/8533de8d-9be2-4bc9-9180-e3cd8d7f3386)

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