FDA Inspection 675579 - Oculus Optikgeraete GMBH - June 24, 2010

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Record Details

This FDA Inspection record concerns Oculus Optikgeraete GMBH, with an inspection on June 24, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company: Oculus Optikgeraete GMBH
Inspection Date: June 24, 2010
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · aa16ecc0-8ad8-4caf-94aa-fe6de3a25e41

Violation Codes1

21 CFR 820.40(a)

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