FDA Inspection 1019036 - Moximed, Inc. - July 07, 2017

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Record Details

This FDA Inspection record concerns Moximed, Inc., with an inspection on July 7, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Moximed, Inc.
Inspection Date: July 7, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · b1e6d9c4-ab12-43d8-9a88-da5519f9ecd7

Violation Codes3

21 CFR 812.4021 CFR 812.43(a)21 CFR 812.43(c)

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