FDA Inspection 1106253 - AndersonBrecon Inc. - September 04, 2019

FDA Inspection 1106253 for AndersonBrecon Inc. on September 04, 2019. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1106253 for AndersonBrecon Inc. on September 04, 2019. Classification: No Action Indicated (NAI).

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Record Information

Company

AndersonBrecon Inc.

Inspection Date

September 4, 2019

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: e63d5921-4ec9-4505-9edd-e32d73f0b81a

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