FDA WARNING_LETTER - Hiossen Inc. - May 16, 2012

FDA WARNING_LETTER for Hiossen Inc. on May 16, 2012. Product: Devices. Access full analysis and detailed observations.

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Record Summary

FDA WARNING_LETTER for Hiossen Inc. on May 16, 2012. Product: Devices. Access full analysis and detailed observations.

Violation Codes

21 U.S.C. 321(h)

21 CFR 820.198(a)

21 CFR 820.75(a)

21 CFR 820.30(f)

21 U.S.C. 351(h)

21 CFR 820.30(g)

21 CFR 820.20(a)

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Record Information

Company

Hiossen Inc.

Inspection Date

May 16, 2012

Product Type

Devices

Office

Department of Health and Human Services

People

Kirk D. Sooter (District Director)

ID: f08ee912-2e5a-4638-8861-8b58a7f6cdc4

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