FDA Inspection 1120306 - ONCORE - SAN MARCOS dba NEOTECH - March 06, 2020

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Record Details

This FDA Inspection record concerns ONCORE - SAN MARCOS dba NEOTECH, with an inspection on March 6, 2020, issued by the Center for Devices and Radiological Health, covering devices.

Company: ONCORE - SAN MARCOS dba NEOTECH
Inspection Date: March 6, 2020
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 8a5680ef-53a3-48f6-ac1f-df76bbbbb3ba

Violation Codes3

21 CFR 820.198(a)21 CFR 820.70(a)21 CFR 820.90(a)

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