FDA Inspection 970549 - Diazyme Laboratories - April 20, 2016

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Record Details

This FDA Inspection record concerns Diazyme Laboratories, with an inspection on April 20, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Diazyme Laboratories
Inspection Date: April 20, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · b65bcbda-5b93-4269-8d13-a2d55d047149

Violation Codes2

21 CFR 820.100(a)21 CFR 820.184

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