FDA Inspection 750677 - Omron Healthcare Co., Ltd - October 06, 2011

FDA Inspection 750677 for Omron Healthcare Co., Ltd on October 06, 2011. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 750677 for Omron Healthcare Co., Ltd on October 06, 2011. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(a)

21 CFR 820.198(a)

21 CFR 820.198(b)

21 CFR 820.250(b)

21 CFR 820.70(c)

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Record Information

Company

Omron Healthcare Co., Ltd

Inspection Date

October 6, 2011

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fc16695b-f89a-443f-886d-480373d9a3b9

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