FDA Inspection 878759 - Acuderm, Inc. - May 09, 2014

FDA Inspection 878759 for Acuderm, Inc. on May 09, 2014. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 878759 for Acuderm, Inc. on May 09, 2014. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(b)

21 CFR 820.22

21 CFR 820.50

21 CFR 820.72(a)

21 CFR 820.75(a)

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Record Information

Company

Acuderm, Inc.

Inspection Date

May 9, 2014

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fc45bf3e-8f2e-4760-89f4-6e6307c32c6f

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