Home » Endoscope Makers Asked by US FDA to Help Improve Device Reprocessing
Endoscope Makers Asked by US FDA to Help Improve Device Reprocessing
December 14, 2009
Manufacturers’ instructions for processing flexible endoscopes need to be accessible, clear and easy to understand to help avert processing errors
that could endanger patients, the U.S. Food and Drug Administration (FDA) says in a safety communication.
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