FDA Inspection 1007422 - OMNIA, Inc. - March 28, 2017

FDA Inspection 1007422 for OMNIA, Inc. on March 28, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1007422 for OMNIA, Inc. on March 28, 2017. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.17

21 CFR 820.22

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Record Information

Company

OMNIA, Inc.

Inspection Date

March 28, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f75e2d77-65cf-4d74-930e-6c996208568b

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