FDA WARNING_LETTER - Superior Products, Inc. - October 31, 2007

FDA WARNING_LETTER for Superior Products, Inc. on October 31, 2007. Product: Devices. Access full analysis and detailed observations.

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Record Summary

FDA WARNING_LETTER for Superior Products, Inc. on October 31, 2007. Product: Devices. Access full analysis and detailed observations.

Violation Codes

21 CFR 820.50(a)(1)

21 CFR 820.30

21 CFR 820.40(a)

21 U.S.C. 321(h)

21 CFR 820.100(a)(4)

21 CFR 820.90(a)

21 CFR 820.198(c)

21 CFR 820.30(b)

21 CFR 820.30(c)

21 CFR 820.75(a)

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Record Information

Company

Superior Products, Inc.

Inspection Date

October 31, 2007

Product Type

Devices

Office

Cincinnati District Office

People

Carol A. Heppe (District Director)

ID: 17436b50-dc74-43b2-9dd8-0f2a667b2d8e

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