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FDA Inspection
•Dornier Medtech Laser GmbH•July 20, 2017

FDA Inspection 1026433 - Dornier Medtech Laser GmbH - July 20, 2017

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Record Details

This FDA Inspection record concerns Dornier Medtech Laser GmbH, with an inspection on July 20, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Dornier Medtech Laser GmbH
Inspection Date
July 20, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
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ID · 89905778-3885-4ae4-93ec-a225e0b0cb62

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