FDA Inspection 819586 - Wavelight GmbH - January 31, 2013

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Record Details

This FDA Inspection record concerns Wavelight GmbH, with an inspection on January 31, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Wavelight GmbH
Inspection Date: January 31, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · e02d01a9-80cc-41fe-ba00-f80b4a4aedb0

Violation Codes1

21 CFR 820.100(a)

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