Introduction
Storage 1
1.5 Storage
Storage of Victoreen instruments must comply with level B storage requirements as outlined in ANSI N45.2.2 (1972) Section 6.1.2(.2). The storage area shall comply with ANSI N45.2.2 (1972) Section 6.2 Storage Area, paragraphs 6.2.1 through 6.2.5. Housekeeping shall conform to ANSI N45.2.3 (1972).
Level B components shall be stored within a fire resistant, tear resistant, weather tight enclosure in a well- ventilated building.
Storage of Victoreen instruments must comply with the following:
1.Inspection and examination of items in storage must be in accordance with ANSI N45.2.2 (1972) Section 6.4.1.
2.Requirements for proper storage must be documented and written procedures or instructions must be established.
3.In the event of fire,
4.Removal of items from storage must be in accordance with ANSI N45.2.2 (1972), Sections 6.5 and 6.6.
1.6 Procedures, Warnings, and Cautions
The equipment described in this manual is intended to be used for the detection and measurement of ionizing radiation. It should be used only by persons who have been trained in the proper interpretation of its readings and the appropriate safety procedures to be followed in the presence of radiation.
Although the equipment described in this manual is designed and manufactured in compliance with all applicable safety standards, certain hazards are inherent in the use of electronic and radiometric equipment.
WARNINGS and CAUTIONS are presented throughout this document to alert the user to potentially hazardous situations. A WARNING is a precautionary message preceding an operation that has the potential to cause personal injury or death. A CAUTION is a precautionary message preceding an operation that has the potential to cause permanent damage to the equipment and/or loss of data. Failure to comply with WARNINGS and CAUTIONS is at the user's own risk and is sufficient cause to terminate the warranty agreement between Fluke Biomedical and the customer.
Adequate warnings are included in this manual and on the product itself to cover hazards that may be encountered in normal use and servicing of this equipment. No other procedures are warranted by Fluke Biomedical. It shall be the owner’s or user's responsibility to see to it that the procedures described here are meticulously followed, and especially that WARNINGS and CAUTIONS are heeded. Failure on the part of the owner or user in any way to follow the prescribed procedures shall absolve Fluke Biomedical and its agents from any resulting liability.
Indicated battery and other operational tests must be performed prior to each use to assure that the instrument is functioning properly. If applicable, failure to conduct periodic performance tests in accordance with ANSI
