FDA Inspection 1249155 - Simex Medizintechnik Gmbh - September 04, 2024

Record Details

This FDA Inspection record concerns Simex Medizintechnik Gmbh, with an inspection on September 4, 2024, issued by the Center for Devices and Radiological Health, covering devices.

Company: Simex Medizintechnik Gmbh
Inspection Date: September 4, 2024
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 88c16460-da59-4388-8259-3940a8ff0d6e

Violation Codes2

21 CFR 820.198(a)21 CFR 820.50

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