FDA Inspection 1051603 - Angiomed GmbH & Co. Medizintechnik KG - April 12, 2018

FDA Inspection 1051603 for Angiomed GmbH & Co. Medizintechnik KG on April 12, 2018. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1051603 for Angiomed GmbH & Co. Medizintechnik KG on April 12, 2018. Classification: No Action Indicated (NAI).

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Record Information

Company

Angiomed GmbH & Co. Medizintechnik KG

Inspection Date

April 12, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fa5eeb6a-7ce0-4f71-bf5e-a011088f4182

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