FDA Inspection 1226348 - Greiner Bio-One GmbH - December 21, 2023

FDA Inspection 1226348 for Greiner Bio-One GmbH on December 21, 2023. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1226348 for Greiner Bio-One GmbH on December 21, 2023. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.17

21 CFR 820.198(a)

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Record Information

Company

Greiner Bio-One GmbH

Inspection Date

December 21, 2023

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 45ce6c33-56f9-447d-8e79-9517098ab896

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