FDA Inspection 1084222 - KATALYST, Inc. - March 28, 2019

FDA Inspection 1084222 for KATALYST, Inc. on March 28, 2019. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1084222 for KATALYST, Inc. on March 28, 2019. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

KATALYST, Inc.

Inspection Date

March 28, 2019

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f8a8de21-441a-47b8-972a-4c25b9bb23a3

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