FDA Inspection
KREWE DU OPTICFDA Inspection 1017591 - KREWE DU OPTIC - November 01, 2016
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Record Details
This FDA Inspection record concerns KREWE DU OPTIC, with an inspection on November 1, 2016, issued by the Center for Devices and Radiological Health, covering devices.
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ID · e4e2ac88-b814-4f65-9c54-97833111335e