FDA Inspection 843178 - Vitalitec International, Inc. - July 19, 2013

FDA Inspection 843178 for Vitalitec International, Inc. on July 19, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 843178 for Vitalitec International, Inc. on July 19, 2013. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.40(a)

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Record Information

Company

Vitalitec International, Inc.

Inspection Date

July 19, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fc1da518-73cf-45c2-a62f-b94ddec7d5ce

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