{"data":{"id":"us/10-cfr-35.2630","jurisdiction":"us","citation":"10 CFR 35.2630","heading":"Records of dosimetry equipment used with remote afterloader units, teletherapy units, and gamma stereotactic radiosurgery units.","body":"(a) A licensee shall retain a record of the calibration, intercomparison, and comparisons of its dosimetry equipment done in accordance with § 35.630 for the duration of the license.\n(b) For each calibration, intercomparison, or comparison, the record must include—\n(1) The date;\n(2) The manufacturer's name, model numbers and serial numbers of the instruments that were calibrated, intercompared, or compared as required by paragraphs (a) and (b) of § 35.630;\n(3) The correction factor that was determined from the calibration or comparison or the apparent correction factor that was determined from an intercomparison; and\n(4) The names of the individuals who performed the calibration, intercomparison, or comparison.","path":["Title 10—Energy","CHAPTER I—NUCLEAR REGULATORY COMMISSION","PART 35—MEDICAL USE OF BYPRODUCT MATERIAL","Subpart L—Records"],"source_url":"https://www.ecfr.gov/api/versioner/v1/full/2026-08-25/title-10.xml","current_through":"2026-08-25","vintage":"","retrieved_at":"2026-08-27T02:24:09Z","sha256":"7800723fec7fb3ac62c78cefe3b138f8ab1d5f3c40b3bebc105cae1efedec59f","source_id":"us-cfr","stale":true,"prev":"us/10-cfr-35.2610","next":"us/10-cfr-35.2632"},"notice":"GroundRules: Original legal text. Not legal advice."}