FDA Inspection 1097388 - Leonhard Lang Medizintechnik GmbH - July 24, 2019

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Record Details

This FDA Inspection record concerns Leonhard Lang Medizintechnik GmbH, with an inspection on July 24, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: Leonhard Lang Medizintechnik GmbH
Inspection Date: July 24, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 1f965b2d-c37d-4176-9239-2e06a7816250

Violation Codes2

21 CFR 820.18421 CFR 820.20(b)

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