FDA Inspection 906360 - Wellell Inc - November 07, 2014

FDA Inspection 906360 for Wellell Inc on November 07, 2014. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 906360 for Wellell Inc on November 07, 2014. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Wellell Inc

Inspection Date

November 7, 2014

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fd38c509-34b0-4a49-8839-bb5a4054c24f

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