FDA Inspection 991500 - Radiometer Basel AG - October 20, 2016

FDA Inspection 991500 for Radiometer Basel AG on October 20, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 991500 for Radiometer Basel AG on October 20, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Radiometer Basel AG

Inspection Date

October 20, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f744b06f-930c-4da2-bcf1-272b49b2709f

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