FDA Inspection 955255 - Kinetic Instruments, Inc. - January 06, 2016

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Record Details

This FDA Inspection record concerns Kinetic Instruments, Inc., with an inspection on January 6, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Kinetic Instruments, Inc.
Inspection Date: January 6, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · c22f1f78-8f83-4356-86a3-779b563f6500

Violation Codes2

21 CFR 803.1721 CFR 820.198(a)

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