BK Meditech Co., Ltd.January 10, 2020

FDA 483 - BK Meditech Co., Ltd. - January 10, 2020

FDA 483 for BK Meditech Co., Ltd. on January 10, 2020. Product: device. Access full analysis and detailed observations.

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Record Summary

FDA 483 for BK Meditech Co., Ltd. on January 10, 2020. Product: device. Access full analysis and detailed observations.

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Record Information

Company

BK Meditech Co., Ltd.

Inspection Date

January 10, 2020

Product Type

device

Office

Division of Clinical Evidence and Analysis 1 (Clinical Policy and Quality)

People

Thai T. Duong

ID: 175f56e6-9079-4684-b4df-a891b0f118e3

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