FDA Inspection 1020923 - Helmer Inc. - July 31, 2017

FDA Inspection 1020923 for Helmer Inc. on July 31, 2017. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1020923 for Helmer Inc. on July 31, 2017. Classification: No Action Indicated (NAI).

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Record Information

Company

Helmer Inc.

Inspection Date

July 31, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fb5b16f5-6199-4c5b-abe1-5666bd716d4a

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