# FDA Inspection 1263611 - Philips Ultrasound, Inc - March 13, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/philips-ultrasound-inc/460aa86d-96cd-403f-9cec-aae68a4b1d59
Source feed: FDA_Inspections

> FDA Inspection 1263611 for Philips Ultrasound, Inc on March 13, 2025. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1263611
- Company Name: Philips Ultrasound, Inc
- Inspection Date: 2025-03-13
- Classification: Official Action Indicated (OAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices

## Related Documents

- [FDA Inspection 1263611 - 2025-03-13](https://www.globalkeysolutions.net/records/fda_inspections/philips-ultrasound-inc/9d43698d-0f91-4d3c-9010-cd1a11a6abbe)
- [FDA Inspection 1263611 - 2025-03-13](https://www.globalkeysolutions.net/records/fda_inspections/philips-ultrasound-inc/84826683-9c7f-43ba-9a5d-1a5af1b5b12c)
- [FDA Inspection 1263611 - 2025-03-13](https://www.globalkeysolutions.net/records/fda_inspections/philips-ultrasound-inc/b122c381-8a77-4e46-9569-f3d44fb2f450)
- [FDA Inspection 797414 - 2012-09-05](https://www.globalkeysolutions.net/records/fda_inspections/philips-ultrasound-inc/e6d45fc1-799a-4ef9-b18c-1d408d3ebdd2)

Company: https://www.globalkeysolutions.net/companies/philips-ultrasound-inc/878735c5-b993-485d-a94d-0b8a86561d37