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U.S. Department of Health and Human Services

Radiation-Emitting Products

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We are applying to become a new FFDM certified facility. We know that we have to perform an MEE on the unit prior to clinical use. However, we will have our examinations read off-site using a review workstation and laser printer (accessory components) that are currently located at another certified facility. Those accessory components have already undergone an MEE as part of the other facility.

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Same answer as in Question 11.

Back to Other Modalities Quality Control Tests

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