# Philips Ultrasound, Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/philips-ultrasound-inc/36d048c6-d991-443c-b562-f9d7bacc8be8

> Inspection records and compliance data for Philips Ultrasound, Inc. in Bothell, Washington. Access full analysis and detailed observations.

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## Details

- Name: Philips Ultrasound, Inc.
- FEI Number: 3019216
- City: Bothell
- State: Washington
- Country Name: United States
- Address Line 1: 22100 Bothell Everett Hwy
- Zip Code: 98021

## Related Documents

- [483 - Philips Ultrasound, Inc. - 2025-01-31](https://www.globalkeysolutions.net/records/483/philips-ultrasound-inc/0bf17fee-3ec3-48b9-9b1f-9ca5f7baf873) — source: FDA, date: January 31, 2025
- [FDA Inspection 1253946 - Philips Ultrasound, Inc. - 2025-01-31](https://www.globalkeysolutions.net/records/fda_inspections/philips-ultrasound-inc/d305636a-d845-4c17-b8e3-7412e16c8d73) — classification: Official Action Indicated (OAI), source: FDA, date: January 31, 2025
- [FDA Inspection 1253946 - Philips Ultrasound, Inc. - 2025-01-31](https://www.globalkeysolutions.net/records/fda_inspections/philips-ultrasound-inc/503d68d3-60d4-44d7-ba3c-21d642b7a3a6) — classification: Official Action Indicated (OAI), source: FDA, date: January 31, 2025
- [FDA Inspection 1253946 - Philips Ultrasound, Inc. - 2025-01-31](https://www.globalkeysolutions.net/records/fda_inspections/philips-ultrasound-inc/49199735-78fa-44ec-9fd3-c809697e64c2) — classification: Official Action Indicated (OAI), source: FDA, date: January 31, 2025
- [FDA Inspection 1253946 - Philips Ultrasound, Inc. - 2025-01-31](https://www.globalkeysolutions.net/records/fda_inspections/philips-ultrasound-inc/566a8308-edd5-40cc-bdaf-b7a67de11f96) — classification: Official Action Indicated (OAI), source: FDA, date: January 31, 2025
- [FDA Inspection 1253946 - Philips Ultrasound, Inc. - 2025-01-31](https://www.globalkeysolutions.net/records/fda_inspections/philips-ultrasound-inc/80fcf747-4b10-4e6e-a780-d39bf8723582) — classification: Official Action Indicated (OAI), source: FDA, date: January 31, 2025
- [FDA Inspection 1253946 - Philips Ultrasound, Inc. - 2025-01-31](https://www.globalkeysolutions.net/records/fda_inspections/philips-ultrasound-inc/a8b2b242-80db-413e-8902-4ee0c69e5188) — classification: Official Action Indicated (OAI), source: FDA, date: January 31, 2025
- [FDA Inspection 1157069 - Philips Ultrasound, Inc. - 2021-11-10](https://www.globalkeysolutions.net/records/fda_inspections/philips-ultrasound-inc/65050dbb-49b1-4d34-8859-b7ed6549a5b9) — classification: No Action Indicated (NAI), source: FDA, date: November 10, 2021
- [FDA Inspection 1157069 - Philips Ultrasound, Inc. - 2021-11-10](https://www.globalkeysolutions.net/records/fda_inspections/philips-ultrasound-inc/b1e51c28-5f5a-4bb1-a765-1e67e7eca466) — classification: No Action Indicated (NAI), source: FDA, date: November 10, 2021
- [FDA Inspection 761739 - Philips Ultrasound, Inc. - 2011-12-09](https://www.globalkeysolutions.net/records/fda_inspections/philips-ultrasound-inc/2705b8c6-1fbf-4e2a-84d6-3082216e984c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 9, 2011
- [FDA Inspection 761739 - Philips Ultrasound, Inc. - 2011-12-09](https://www.globalkeysolutions.net/records/fda_inspections/philips-ultrasound-inc/51fecd2b-2e1f-4c13-89af-c20ab779a51c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 9, 2011

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