FDA Inspection 1000040 - Atlantic Horizon International, Inc. - December 07, 2016

FDA Inspection 1000040 for Atlantic Horizon International, Inc. on December 07, 2016. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1000040 for Atlantic Horizon International, Inc. on December 07, 2016. Classification: No Action Indicated (NAI).

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Record Information

Company

Atlantic Horizon International, Inc.

Inspection Date

December 7, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f72aef52-e4e8-47b4-9c6a-bd67ecbb053b

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