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COMPLIANCE INFO_1980-2010
EnvironmentalHealth
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4500 - Medical Waste Program
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PR0450003
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COMPLIANCE INFO_1980-2010
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Last modified
2/25/2026 2:54:44 PM
Creation date
7/3/2020 10:17:08 AM
Metadata
Fields
Template:
EHD - Public
ProgramCode
4500 - Medical Waste Program
File Section
COMPLIANCE INFO
FileName_PostFix
1980-2010
RECORD_ID
PR0450003
PE
4522 - ACUTE CARE FACILITY
FACILITY_ID
FA0000513
FACILITY_NAME
LODI MEMORIAL HOSPITAL
STREET_NUMBER
975
Direction
S
STREET_NAME
FAIRMONT
STREET_TYPE
AVE
City
LODI
Zip
95240
APN
03107039
CURRENT_STATUS
Active, billable
SITE_LOCATION
975 S FAIRMONT AVE
P_LOCATION
02
P_DISTRICT
004
QC Status
Approved
Scanner
SJGOV\cfield
Supplemental fields
FilePath
\MIGRATIONS\MW\MW_4522_PR0450003_975 S FAIRMONT_1980-2010.tif
Site Address
975 S FAIRMONT AVE LODI 95240
Tags
EHD - Public
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0 <br />State of California -Health and Human Servgency Department of Health Services <br />Page 4 of 5 pages <br />License Number: 1368-39 <br />Amendment Number: 30 <br />20. The licensee may use one constancy source for the dose calibrator constancy test provided that the dose <br />calibrator manual indicates that only one constancy source is needed for proper Quality Control. <br />21. The licensee may use any commercially available device, acceptable to the U.S. Nuclear Regulatory Commission, an <br />Agreement State or a Licensing State, for doing linearity tests of its dose calibrator provided the procedures <br />described by the manufacturer of the linearity device are followed. <br />22. Nuclear medicine technology procedures shall be performed by nuclear medicine technologists pursuant to Title 17, <br />California Code of Regulations, Subchapter 4.6. Such procedures shall be performed under the supervision of <br />individuals listed as authorized users on this license who meet the criteria specified in Section 30510. Certificates or <br />special permits issued pursuant to Subchapter 4.6 shall be prominently displayed at the facility authorized on this <br />license. <br />23. Treatment and management of patients receiving therapeutic quantities of unsealed radioactive materials <br />shall be in accordance with the guidance from any of the following: <br />(a) Chapter 4, "Release from Hospital of Patients Containing Radioactive Material" National Council on <br />Radiation Protection and Measurements (NCRP) Report No. 37, "Precautions in the Management of <br />Patients Who Have Received Therapeutic Amounts of Radionuclides" (NCRP Publications, P.O. Box <br />30175, Washington, D.C. 20014). <br />(b) Appendix M in the "Guide for the Preparation of Applications for Medical Programs", State of <br />California, Department of Health Services, Radiological Health Branch. <br />(c) Documented rationale or patient -specific calculations demonstrating that members of the general public <br />will be limited to 500 mrem total effective dose equivalent from patients who have been released <br />containing therapeutic quantities of radiopharmaceuticals. <br />24. Treatment and management of patients undergoing brachytherapy shall be in accordance with the guidance <br />from any of the following: <br />(a) Chapter 5, "Safety Precautions in Clinical Application", National Council on Radiation Protection and <br />Measurements (NCRP) Report No. 40, "Protection Against Radiation From Brachytherapy Sources" <br />(NCRP Publications, P.O. Box 30175, Washington, D.C. 20014). <br />b) ADpendix N in the "Guide for the Preparation of Applications for . Medical Programs", State of <br />California, Department of Health Services, Radiological Health Branch. <br />(c) Documented rationale or patient -specific calculations demonstrating that members of the general public <br />will be limited to 500 mrem total effective dose equivalent from patients who have been released <br />containing therapeutic quantities of radionuclides. <br />25. If there is reason to suspect that a medical radium source may be leaking or contaminated, it shall be tested before <br />further use, by a method acceptable to the Department of Health Services, and a report of the test results and the <br />action taken shall be submitted within 30 days to the Radiologic Health Branch. <br />26. Production or processing of radiopharmaceuticals for the purpose of commercial distribution to other licensees is not <br />authorized by this license. <br />
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