ML22249A127

Shine Technologies, LLC Final Safety Analysis Report, Chapter 10, Rev. 0, Experimental Facilities

ML22249A127
Person / Time
Site:	SHINE Medical Technologies
Issue date:	08/31/2022
From:	SHINE Technologies, SHINE Health. Illuminated
To:	Office of Nuclear Reactor Regulation
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Text

Chapter 10 - Experimental Facilities Table of Contents

CHAPTER 10

EXPERIMENTAL FACILITIES

TABLE OF CONTENTS

Section Tit le 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 Tit le None

SHINE Medical Technologies 10-ii Rev. 0 Chapter 10 - Experimental Facilities List of Figures

LIST OF FIGURES

Number Tit le 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 Applicatio ns 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