FDA Inspection 1000062 - OMNIA SRL - December 15, 2016

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Record Details

This FDA Inspection record concerns OMNIA SRL, with an inspection on December 15, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: OMNIA SRL
Inspection Date: December 15, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · aa22d294-2ca7-4e4f-8315-51908cabb420