FDA WARNING_LETTER - Transdermal Cap Inc. - June 30, 2015

FDA WARNING_LETTER for Transdermal Cap Inc. on June 30, 2015. Product: Devices. Access full analysis and detailed observations.

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Record Summary

FDA WARNING_LETTER for Transdermal Cap Inc. on June 30, 2015. Product: Devices. Access full analysis and detailed observations.

Violation Codes

21 CFR 820.100(a)

21 CFR 820

21 U.S.C. 321(h)

21 CFR 820.100(a)(1)

21 CFR 820.90(a)

21 CFR 820.198(a)

21 CFR 820.198(c)

21 CFR 820.30(f)

21 CFR 820.50

21 U.S.C. 351(h)

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Record Information

Company

Transdermal Cap Inc.

Inspection Date

June 30, 2015

Product Type

Devices

Office

Cincinnati District Office

People

Toniette K. Williams (Director)

ID: f58e0eee-ad95-4dae-bcf6-07941c49ac70

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