# FDA Inspection 1024590 - Livedo Usa, Inc. - July 19, 2017

Source: https://www.keypedia.com/records/fda_inspections/livedo-usa-inc/26e1df49-dd23-4cfe-b188-4e803b64f4b8
Source feed: FDA_Inspections

> FDA Inspection 1024590 for Livedo Usa, Inc. on July 19, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1024590
- Company Name: Livedo Usa, Inc.
- Inspection Date: 2017-07-19
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1024590 - 2017-07-19](https://www.keypedia.com/records/fda_inspections/livedo-usa-inc/07579ff6-b290-4ee9-9b33-6339bf6c5a1b)

Company: https://www.keypedia.com/companies/livedo-usa-inc/d384b6b0-4b6f-435a-8285-92ae58636952

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