FDA Inspection 584472 - Bloomex International, Inc. - May 01, 2009

FDA Inspection 584472 for Bloomex International, Inc. on May 01, 2009. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 584472 for Bloomex International, Inc. on May 01, 2009. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.17

21 CFR 820.100(b)

21 CFR 820.198(a)

21 CFR 820.20(b)(3)

21 CFR 820.20(c)

21 CFR 820.22

21 CFR 820.30(i)

21 CFR 820.72(a)

21 CFR 820.80(a)

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Record Information

Company

Bloomex International, Inc.

Inspection Date

May 1, 2009

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fa7e51ca-ce12-4a5f-909e-b6168528fd32

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