FDA Inspection 789275 - EMG Manufacturing Co., Ltd. - June 14, 2012

FDA Inspection 789275 for EMG Manufacturing Co., Ltd. on June 14, 2012. Classification: Official Action Indicated (OAI).

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Record Summary

FDA Inspection 789275 for EMG Manufacturing Co., Ltd. on June 14, 2012. Classification: Official Action Indicated (OAI).

Violation Codes

21 CFR 803.17

21 CFR 820.184

21 CFR 820.198(a)

21 CFR 820.250(b)

21 CFR 820.30(g)

21 CFR 820.70(c)

21 CFR 820.80(c)

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Record Information

Company

EMG Manufacturing Co., Ltd.

Inspection Date

June 14, 2012

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f937260e-fb15-4ebf-b74a-dea6e993c312

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