FDA Inspection 998293 - Oculus Optikgeraete GMBH - November 10, 2016

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Record Details

This FDA Inspection record concerns Oculus Optikgeraete GMBH, with an inspection on November 10, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Oculus Optikgeraete GMBH
Inspection Date: November 10, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · e328a026-18a4-4d5c-a2a1-74551572b143