FDA Inspection 575847 - Radiometer Basel AG - March 26, 2009

FDA Inspection 575847 for Radiometer Basel AG on March 26, 2009. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 575847 for Radiometer Basel AG on March 26, 2009. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Radiometer Basel AG

Inspection Date

March 26, 2009

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 66588f76-8071-497b-a8ba-606133965cb9

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