# FDA Inspection 1247774 - Philips Ultrasound, Inc. - August 08, 2024

Source: https://www.keypedia.com/records/fda_inspections/philips-ultrasound-inc/95408ce7-264b-49da-a089-074039d9291d
Source feed: FDA_Inspections

> FDA Inspection 1247774 for Philips Ultrasound, Inc. on August 08, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1247774
- Company Name: Philips Ultrasound, Inc.
- Inspection Date: 2024-08-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1247774 - 2024-08-08](https://www.keypedia.com/records/fda_inspections/philips-ultrasound-inc/057641c1-113a-4645-a396-ea249de9f6d0)

Company: https://www.keypedia.com/companies/philips-ultrasound-inc/51274bc5-1ed8-4dc2-a0e2-ef8525450d80

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