FDA Inspection 1020669 - Kwivik Medical, Inc. - July 25, 2017

FDA Inspection 1020669 for Kwivik Medical, Inc. on July 25, 2017. Classification: Official Action Indicated (OAI).

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Record Summary

FDA Inspection 1020669 for Kwivik Medical, Inc. on July 25, 2017. Classification: Official Action Indicated (OAI).

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Record Information

Company

Kwivik Medical, Inc.

Inspection Date

July 25, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fe4bd546-db58-46c1-beb8-29353fee6def

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