FDA Inspection 1192167 - Gulden Ophthalmics - October 27, 2022

FDA Inspection 1192167 for Gulden Ophthalmics on October 27, 2022. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1192167 for Gulden Ophthalmics on October 27, 2022. Classification: No Action Indicated (NAI).

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Record Information

Company

Gulden Ophthalmics

Inspection Date

October 27, 2022

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fc1dd314-8352-4780-a5f8-2d60dba57c3b

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