Volume 43, Issue 16, Page 8 (15 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 at 800-332-1088 or www.fda.gov/MedWatch/report.htm.
PII: S0029-7437(08)70525-1
doi:10.1016/S0029-7437(08)70525-1
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