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

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

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Record Summary

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

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Record Information

Company

Sebia, Inc.

Inspection Date

June 28, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: ff237cee-aaff-419c-8792-dc25824bc44d

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