FDA Inspection 1054723 - Mobius Medical Systems, LP - June 07, 2018

FDA Inspection 1054723 for Mobius Medical Systems, LP on June 07, 2018. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1054723 for Mobius Medical Systems, LP on June 07, 2018. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Mobius Medical Systems, LP

Inspection Date

June 7, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f8beab0f-eb5c-4396-929f-65f695eac33c

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