FDA Inspection 1060993 - Omnitech Systems, Inc. - June 13, 2018

FDA Inspection 1060993 for Omnitech Systems, Inc. on June 13, 2018. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1060993 for Omnitech Systems, Inc. on June 13, 2018. Classification: No Action Indicated (NAI).

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Record Information

Company

Omnitech Systems, Inc.

Inspection Date

June 13, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fe54bdcd-6c7e-48ee-a371-287eb614866b

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