A licensee must retain a record of the calibrations, intercomparisons, and comparisons of dosimetry equipment required under part 4731.4468 for the duration of the license. For each calibration, intercomparison, or comparison, the record must include:
B. the manufacturer's name, model number, and serial number for the instrument that was calibrated, intercompared, or compared;C. the correction factor that was determined from the calibration or comparison or the apparent correction factor that was determined from an intercomparison; andD. the name of the individual who performed the calibration, intercomparison, or comparison.Minn. R. agency 144, ch. 4731, MEDICAL USE OF RADIOACTIVE MATERIAL, pt. 4731.4517
Statutory Authority: MS s 144.1202; 144.1203