FDA Inspection 1052173 - Wondfo USA Co Ltd - May 11, 2018

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Record Details

This FDA Inspection record concerns Wondfo USA Co Ltd, with an inspection on May 11, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Wondfo USA Co Ltd
Inspection Date: May 11, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 85d2571d-dfab-4a91-8a7e-eaf9a7688b8f

Violation Codes4

21 CFR 803.1721 CFR 820.198(a)21 CFR 820.25(a)21 CFR 820.40(a)

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