FDA Inspection 1220148 - Remeda AB - September 14, 2023

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Record Details

This FDA Inspection record concerns Remeda AB, with an inspection on September 14, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company: Remeda AB
Inspection Date: September 14, 2023
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 0a7b7afe-87c1-49c9-ba8a-bb8d75a4aa54

Violation Codes1

21 CFR 820.90(b)(2)

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