FDA Inspection 1195668 - BM Korea Co. Ltd. - January 18, 2023

FDA Inspection 1195668 for BM Korea Co. Ltd. on January 18, 2023. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1195668 for BM Korea Co. Ltd. on January 18, 2023. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(b)

21 CFR 820.198(a)

21 CFR 820.70(c)

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Record Information

Company

BM Korea Co. Ltd.

Inspection Date

January 18, 2023

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fd69a524-618f-4b03-9a41-e0844e78902e

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