FDA Inspection 1022305 - Ducommun Labarge Technologies - August 11, 2017

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Record Details

This FDA Inspection record concerns Ducommun Labarge Technologies, with an inspection on August 11, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Ducommun Labarge Technologies
Inspection Date: August 11, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 83d79da1-589a-449c-8e37-2bfd73f2f8d3

Violation Codes3

21 CFR 820.18121 CFR 820.2221 CFR 820.75(a)

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