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483
•Itamar Medical, Ltd.•December 20, 2018

FDA 483 - Itamar Medical, Ltd. - December 20, 2018

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Record Details

This FDA Form 483 report for Itamar Medical, Ltd. indicates no inspectional observations were noted during the inspection. The inspection found no significant issues requiring corrective action.

Company
Itamar Medical, Ltd.
Inspection Date
December 20, 2018
Product Type
Device
Office
Human Foods Program
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ID · 6f445ddf-f6d7-4d91-8109-3625283f639d

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