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

Record Details

This FDA Inspection record concerns OMNIA, Inc., with an inspection on March 28, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: OMNIA, Inc.
Inspection Date: March 28, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · ddc69264-3224-4484-91af-c4f18410ce53

Violation Codes2

21 CFR 803.1721 CFR 820.22

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