# Philips North America - Inspection Records

Source: https://www.globalkeysolutions.net/companies/philips-north-america/62465dd7-c599-42c6-bd2e-5794bc5f4de2

> Inspection records and compliance data for Philips North America in Cambridge, Massachusetts. Access full analysis and detailed observations.

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## Details

- Name: Philips North America
- FEI Number: 3006648320
- City: Cambridge
- State: Massachusetts
- Country Name: United States
- Address Line 1: 222 Jacobs St
- Zip Code: 02141

## Related Documents

- [483 - Philips North America - 2023-12-13](https://www.globalkeysolutions.net/records/483/philips-north-america/5d1fb101-85aa-4fbe-ac15-4e3e0c7ccedc) — source: FDA, date: December 13, 2023
- [FDA Inspection 1224855 - Philips North America - 2023-12-13](https://www.globalkeysolutions.net/records/fda_inspections/philips-north-america/c904f90c-ace0-49c7-b3f3-d5212e6e6fdb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 13, 2023
- [FDA Inspection 1224855 - Philips North America - 2023-12-13](https://www.globalkeysolutions.net/records/fda_inspections/philips-north-america/b33e52a2-859e-44c2-ade3-a69a8a614d93) — classification: No Action Indicated (NAI), source: FDA, date: December 13, 2023
- [FDA Inspection 1005211 - Philips North America - 2017-03-03](https://www.globalkeysolutions.net/records/fda_inspections/philips-north-america/e2cb00cf-409d-4f2c-b923-99f98a7a6b0a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 3, 2017
- [FDA Inspection 777361 - Philips North America - 2012-04-13](https://www.globalkeysolutions.net/records/fda_inspections/philips-north-america/30d66b08-2cf6-4bf5-9820-18c0c8f31609) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 13, 2012
- [FDA Inspection 607750 - Philips North America - 2009-07-18](https://www.globalkeysolutions.net/records/fda_inspections/philips-north-america/a332af6f-3b1e-4acf-a072-6780f99f7a32) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 18, 2009
- [FDA Inspection 607750 - Philips North America - 2009-07-18](https://www.globalkeysolutions.net/records/fda_inspections/philips-north-america/04cbccaf-af77-4cb3-8351-5089ebe33898) — classification: No Action Indicated (NAI), source: FDA, date: July 18, 2009

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