FDA Inspection 1063787 - MedFact Engineering GmbH - July 25, 2018

FDA Inspection 1063787 for MedFact Engineering GmbH on July 25, 2018. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1063787 for MedFact Engineering GmbH on July 25, 2018. Classification: No Action Indicated (NAI).

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Record Information

Company

MedFact Engineering GmbH

Inspection Date

July 25, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fce69e94-e30e-462b-9918-12cb16a3d88f

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