FDA Inspection 1221779 - Gyrus ACMI, Inc. - November 02, 2023

FDA Inspection 1221779 for Gyrus ACMI, Inc. on November 02, 2023. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1221779 for Gyrus ACMI, Inc. on November 02, 2023. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(a)

21 CFR 820.184

21 CFR 820.198(a)

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Record Information

Company

Gyrus ACMI, Inc.

Inspection Date

November 2, 2023

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fe9085a2-81a2-4d96-aca0-01d4a7337da9

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