FDA Inspection 808901 - Lombart Instrument, Inc. d/b/a Marco Ophthalmic - November 21, 2012

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Record Details

This FDA Inspection record concerns Lombart Instrument, Inc. d/b/a Marco Ophthalmic, with an inspection on November 21, 2012, issued by the Center for Devices and Radiological Health, covering devices.

Company: Lombart Instrument, Inc. d/b/a Marco Ophthalmic
Inspection Date: November 21, 2012
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · ae3e5551-83ee-40da-8cfc-4e594d4c783f