FDA Inspection 1015641 - Yokowo Co Ltd - April 13, 2017

FDA Inspection 1015641 for Yokowo Co Ltd on April 13, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1015641 for Yokowo Co Ltd on April 13, 2017. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(a)

21 CFR 820.100(b)

21 CFR 820.184

21 CFR 820.30(c)

21 CFR 820.30(f)

21 CFR 820.30(j)

21 CFR 820.40(a)

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Record Information

Company

Yokowo Co Ltd

Inspection Date

April 13, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f85557ec-d962-4780-8021-13d92df71a70

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