FDA Inspection 790206 - Bloomex International, Inc. - July 02, 2012

FDA Inspection 790206 for Bloomex International, Inc. on July 02, 2012. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 790206 for Bloomex International, Inc. on July 02, 2012. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.17

21 CFR 820.20(c)

21 CFR 820.22

21 CFR 820.25(b)

21 CFR 820.30(i)

21 CFR 820.72(a)

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Record Information

Company

Bloomex International, Inc.

Inspection Date

July 2, 2012

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 3462625e-292e-4d95-ba14-299bd1530cb2

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