FDA Inspection 858941 - GETSCH+HILLER MEDIZINTECHNIK GmbH - November 28, 2013

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Record Details

This FDA Inspection record concerns GETSCH+HILLER MEDIZINTECHNIK GmbH, with an inspection on November 28, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: GETSCH+HILLER MEDIZINTECHNIK GmbH
Inspection Date: November 28, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 1052d5eb-a69b-4b06-9dfe-f2e41a03601a

Violation Codes2

21 CFR 820.18421 CFR 820.75(a)

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