FDA Inspection 902924 - Belimed Technik Gmbh - November 13, 2014

FDA Inspection 902924 for Belimed Technik Gmbh on November 13, 2014. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 902924 for Belimed Technik Gmbh on November 13, 2014. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Belimed Technik Gmbh

Inspection Date

November 13, 2014

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fa51708f-5bd0-4bc1-be5c-efa2fc9b3c07

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