FDA Inspection 561290 - OPKO Instrumentation/OTI - January 22, 2009

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Record Details

This FDA Inspection record concerns OPKO Instrumentation/OTI, with an inspection on January 22, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company: OPKO Instrumentation/OTI
Inspection Date: January 22, 2009
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 9beddc84-b56f-40d8-80bf-ba3686893ff9