# FDA Inspection 1003219 - Echosens - February 01, 2017

Source: https://www.keypedia.com/records/fda_inspections/echosens/cec529a7-2fd9-4d95-941c-3acc136f3bb1
Source feed: FDA_Inspections

> FDA Inspection 1003219 for Echosens on February 01, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1003219
- Company Name: Echosens
- Inspection Date: 2017-02-01
- 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 1003219 - 2017-02-01](https://www.keypedia.com/records/fda_inspections/echosens/9c9e32f9-dc42-4e2d-bfc4-5db1e61e3345)

Company: https://www.keypedia.com/companies/echosens/2d8658d3-8a08-4626-8965-42c14fb48513

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