FDA Inspection 1031124 - Moor Instruments Ltd - May 05, 2017

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Record Details

This FDA Inspection record concerns Moor Instruments Ltd, with an inspection on May 5, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Moor Instruments Ltd
Inspection Date: May 5, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 83177dfe-88a9-41af-9465-55368c281cf9

Violation Codes2

21 CFR 820.100(b)21 CFR 820.198(c)

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