ML20105A306

Shine Medical Technologies, LLC, Supplement 2 to License Application, Rev.2 to Final Safety Analysis Report, Chapter 10, Experimental Facilities

ML20105A306
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Site:	SHINE Medical Technologies
Issue date:	03/27/2020
From:	SHINE Medical Technologies
To:	Office of Nuclear Reactor Regulation
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Chapter 10 - Experimental Facilities Table of Contents CHAPTER 10 EXPERIMENTAL FACILITIES TABLE OF CONTENTS Section Title Page 10.1

SUMMARY

DESCRIPTION ............................................................................... 10.1-1

10.2 REFERENCES

................................................................................................... 10.2-1 SHINE Medical Technologies 10-i Rev. 0

Chapter 10 - Experimental Facilities List of Tables LIST OF TABLES Number Title None SHINE Medical Technologies 10-ii Rev. 0

Chapter 10 - Experimental Facilities List of Figures LIST OF FIGURES Number Title None SHINE Medical Technologies 10-iii Rev. 0

Chapter 10 - Experimental Facilities Acronyms and Abbreviations ACRONYMS AND ABBREVIATIONS Acronym/Abbreviation Definition None SHINE Medical Technologies 10-iv Rev. 0

Chapter 10 - Experimental Facilities Summary Description CHAPTER 10 - EXPERIMENTAL FACILITIES 10.1

SUMMARY

DESCRIPTION The SHINE facility does not contain experimental facilities as described in NUREG-1537, Part 1, Guidelines for Preparing and Reviewing Applications for the Licensing of Non-Power Reactors:

Format and Content (USNRC, 1996) and the Interim Staff Guidance Augmenting NUREG-1537, Part 1, Guidelines for Preparing and Reviewing Applications for the Licensing of Non-Power Reactors: Format and Content, for Licensing Radioisotope Production Facilities and Aqueous Homogeneous Reactors (USNRC, 2012).

SHINE Medical Technologies 10.1-1 Rev. 0

Chapter 10 - Experimental Facilities References

10.2 REFERENCES

USNRC, 1996. Guidelines for Preparing and Reviewing Applications for the Licensing of Non-Power Reactors: Format and Content, NUREG-1537, Part 1, U.S. Nuclear Regulatory Commission, February 1996.

USNRC, 2012. Interim Staff Guidance Augmenting NUREG-1537, Part 1, Guidelines for Preparing and Reviewing Applications for the Licensing of Non-Power Reactors: Format and Content, for Licensing Radioisotope Production Facilities and Aqueous Homogeneous Reactors, Interim Staff Guidance Augmenting NUREG-1537, Part 1, U.S. Nuclear Regulatory Commission, October 17, 2012.

SHINE Medical Technologies 10.2-1 Rev. 0