Volume 4, Issue 8, Page 7 (August 2008)
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The notice is available at www.fda.gov/cdrh/safety/071408-ctscanning.html. Adverse events related to CT equipment can be reported to the FDA's MedWatch program at 800-332-1088 or www.fda.gov/MedWatch/report.htm.
PII: S1553-3212(08)70253-X
doi:10.1016/S1553-3212(08)70253-X
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