FDA Inspection 865535 - Mauna Kea Technologies - January 30, 2014

FDA Inspection 865535 for Mauna Kea Technologies on January 30, 2014. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 865535 for Mauna Kea Technologies on January 30, 2014. Classification: No Action Indicated (NAI).

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Record Information

Company

Mauna Kea Technologies

Inspection Date

January 30, 2014

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fabb5384-f05f-4f21-bb76-3bdd89e20e97

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