# FDA Inspection 1020822 - Sebia,  Inc. - June 28, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/sebia-inc/370e7f67-010d-4d54-bb4b-1dd7fda7ef83
Source feed: FDA_Inspections

> FDA Inspection 1020822 for Sebia,  Inc. on June 28, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020822
- Company Name: Sebia,  Inc.
- Inspection Date: 2017-06-28
- 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 1020822 - 2017-06-28](https://www.globalkeysolutions.net/records/fda_inspections/sebia-inc/ff237cee-aaff-419c-8792-dc25824bc44d)

Company: https://www.globalkeysolutions.net/companies/sebia-inc/8fdff428-abf3-4387-a4d5-bf4cdf61f2ec

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