FDA Inspection 1202192 - Konica Minolta, Inc. - April 05, 2023

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Record Details

This FDA Inspection record concerns Konica Minolta, Inc., with an inspection on April 5, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company: Konica Minolta, Inc.
Inspection Date: April 5, 2023
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 821756d2-5a02-48ac-b481-bb4759157d3a

Violation Codes3

21 CFR 820.30(e)21 CFR 820.30(f)21 CFR 820.30(g)

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