FDA Inspection 1270229 - August Reuchlen GmbH - May 02, 2025

Record Details

This FDA Inspection record concerns August Reuchlen GmbH, with an inspection on May 2, 2025, issued by the Center for Devices and Radiological Health, covering devices.

Company: August Reuchlen GmbH
Inspection Date: May 2, 2025
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · ad47d5f9-d5e2-4cb2-8d1e-b104f7ef034c

Violation Codes2

21 CFR 820.100(b)21 CFR 820.50(a)(2)

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