FDA Inspection 1117171 - ARCH-Blandon - February 07, 2020

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Record Details

This FDA Inspection record concerns ARCH-Blandon, with an inspection on February 7, 2020, issued by the Center for Devices and Radiological Health, covering devices.

Company: ARCH-Blandon
Inspection Date: February 7, 2020
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 4adeee57-0790-48ac-9362-4a874d85a843

Violation Codes1

21 CFR 820.72(b)

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