FDA Inspection 1038015 - Venni Instruments Inc - January 17, 2018

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Record Details

This FDA Inspection record concerns Venni Instruments Inc, with an inspection on January 17, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Venni Instruments Inc
Inspection Date: January 17, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 1818e33c-de72-4bec-970e-d981913e9090

Violation Codes1

21 CFR 820.198(e)

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