FDA Inspection 985052 - Beacon Converters, Inc. - September 13, 2016

FDA Inspection 985052 for Beacon Converters, Inc. on September 13, 2016. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 985052 for Beacon Converters, Inc. on September 13, 2016. Classification: No Action Indicated (NAI).

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Record Information

Company

Beacon Converters, Inc.

Inspection Date

September 13, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 95d0bc94-3fbf-42f0-9ae9-8f88a1d4a979

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