FDA Inspection 902925 - EMG Technology Co., Ltd. - October 23, 2014

FDA Inspection 902925 for EMG Technology Co., Ltd. on October 23, 2014. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 902925 for EMG Technology Co., Ltd. on October 23, 2014. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.17(a)(1)

21 CFR 803.50(a)(2)

21 CFR 820.198(c)

21 CFR 820.50(b)

21 CFR 820.80(b)

21 CFR 820.86

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Record Information

Company

EMG Technology Co., Ltd.

Inspection Date

October 23, 2014

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fca7b6f6-824b-4829-ba57-ade9ec4bcf0f

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