FDA Inspection 823920 - ABB, Inc. - March 21, 2013

FDA Inspection 823920 for ABB, Inc. on March 21, 2013. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 823920 for ABB, Inc. on March 21, 2013. Classification: No Action Indicated (NAI).

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Record Information

Company

ABB, Inc.

Inspection Date

March 21, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fcef2ed6-9b2b-4a11-8721-3c9d4925b511

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