FDA Inspection 1053547 - Mauna Kea Technologies - May 17, 2018

FDA Inspection 1053547 for Mauna Kea Technologies on May 17, 2018. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1053547 for Mauna Kea Technologies on May 17, 2018. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Mauna Kea Technologies

Inspection Date

May 17, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 5f3cf109-b885-402a-aee4-6374ce63eb64

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