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U.S. Department of Health and Human Services

Radiation-Emitting Products

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We are adding an FFDM unit to our already certified digital facility. We know that we have to perform an MEE on the unit prior to clinical use. However, since our review workstation and laser printer (accessory components) have already undergone an MEE and are currently being used with our first unit, do they have to undergo a new MEE or can we use their original MEE or a subsequent annual ph...

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Same answer as in Question 11.

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