# FDA Inspection 977943 - KPI  Ultrasound Inc - June 30, 2016

Source: https://www.keypedia.com/records/fda_inspections/kpi-ultrasound-inc/5bf3b160-35ea-46d8-9849-8ae1eafb9319
Source feed: FDA_Inspections

> FDA Inspection 977943 for KPI  Ultrasound Inc on June 30, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 977943
- Company Name: KPI  Ultrasound Inc
- Inspection Date: 2016-06-30
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 977943 - 2016-06-30](https://www.keypedia.com/records/fda_inspections/kpi-ultrasound-inc/a8e7321a-4f57-42a0-955d-6123528ce942)

Company: https://www.keypedia.com/companies/kpi-ultrasound-inc/9e1987c3-8d43-4919-a175-94d42abd0761

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