Stay out of hot water with the FDA
Mammography Regulation and Reimbursement Report, September 1, 2009
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QC problems landed two facilities in trouble with the FDA this spring. One facility had missing QC records and the other failed to follow the digital manufacturer’s QC guidelines. Below is a rundown of what the FDA found and our expert’s tips for avoiding similar problems.
This is an excerpt from a member only article. To read the article in its entirety, please login.
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