Thomas J. Quinn - Citizen Petition
This Other document was issued by the Food and Drug Administration (FDA)
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Date Posted: Aug 30, 2013
Country: United States
Category: Individual Consumer
It is my belief that the FDA should review and update regulations governing MRI devices within their authority. The advances and increased power levels that are...
Any effort to improve the safety of patients, operators and service providers of any medical device should be reviewed by the FDA and implemented as necessary...
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