FDA Inspection 1030456 - Unique Instruments, Inc. - November 01, 2017

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Record Details

This FDA Inspection record concerns Unique Instruments, Inc., with an inspection on November 1, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Unique Instruments, Inc.
Inspection Date: November 1, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 5bb66ff3-0a32-488c-acdf-70f39744ff0a

Violation Codes9

21 CFR 820.100(a)21 CFR 820.198(e)21 CFR 820.70(c)21 CFR 820.70(i)21 CFR 820.75(a)21 CFR 820.75(b)21 CFR 820.80(b)21 CFR 820.80(c)21 CFR 820.90(a)

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FDA Inspection

Unique Instruments, Inc.November 1, 2017