FDA Inspection 915643 - Lepu Medical Technology (Beijing) Co., Ltd. - February 05, 2015

FDA Inspection 915643 for Lepu Medical Technology (Beijing) Co., Ltd. on February 05, 2015. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 915643 for Lepu Medical Technology (Beijing) Co., Ltd. on February 05, 2015. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.198(a)

21 CFR 820.75(b)(2)

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Record Information

Company

Lepu Medical Technology (Beijing) Co., Ltd.

Inspection Date

February 5, 2015

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: e9ae09c2-8311-4e3a-94de-83553b25dbfd

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