FDA Inspection 1283582 - Armbrust Inc. - September 25, 2025

FDA Inspection 1283582 for Armbrust Inc. on September 25, 2025. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1283582 for Armbrust Inc. on September 25, 2025. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.22

21 CFR 820.90(a)

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Record Information

Company

Armbrust Inc.

Inspection Date

September 25, 2025

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: faa9461c-9bb8-4f71-8cc5-90c3af7d25d2

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