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

FDA Inspection 1038015 for Venni Instruments Inc on January 17, 2018. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1038015 for Venni Instruments Inc on January 17, 2018. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.198(e)

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Record Information

Company

Venni Instruments Inc

Inspection Date

January 17, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fe680c97-4eec-4692-909e-0321507460e9

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