FDA Inspection 1035513 - Sterling Diagnostics, Inc. - December 20, 2017

FDA Inspection 1035513 for Sterling Diagnostics, Inc. on December 20, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1035513 for Sterling Diagnostics, Inc. on December 20, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Sterling Diagnostics, Inc.

Inspection Date

December 20, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 857714b5-8fda-41f7-bf42-48b012d28050

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