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May 27, 2004, MAMMOGRAPHY FACILITY ADVERSE EVENT AND ACTION REPORT 2003 BACKGROUND Congress enacted the Mammography Quality Standards Act (MESA) in 1992, marking the first time mammography facilities
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What is mammography facility adverse event?
Mammography facility adverse event refers to any undesired occurrence or incident that happens in a mammography facility during the performance of mammography exams.
Who is required to file mammography facility adverse event?
Mammography facilities are required by law to report any adverse events that occur within their facility.
How to fill out mammography facility adverse event?
The process of filling out a mammography facility adverse event report involves documenting the details of the event, including the date, time, location, individuals involved, and a description of the event.
What is the purpose of mammography facility adverse event?
The purpose of reporting mammography facility adverse events is to ensure patient safety, monitor and address any issues that may arise during mammography exams, and improve the overall quality of mammography services.
What information must be reported on mammography facility adverse event?
The information that must be reported on a mammography facility adverse event includes the date and time of the event, the location of the facility, a description of the event, the individuals involved, and any actions taken in response to the event.
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