# Sebia,  Inc. – FDA Inspection, Jun 28, 2017

Source: https://www.keypedia.com/records/fda_inspections/sebia-inc/ff237cee-aaff-419c-8792-dc25824bc44d
Source feed: FDA_Inspections

> FDA inspection 1020822 of Sebia,  Inc., 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)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Officers

- [Melanie W. Pishnery](https://www.keypedia.com/people/melanie-w-pishnery/ff4846b0-ffe1-4df0-9116-4bb238866b3a)

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

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