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Visit fda's website for a list of authorized tests Laboratory testing can help distinguish whether someone is susceptible to ebv infection or has a recent or past infection Monospot test is not recommended for general use. Laboratory diagnosis of lyme disease relies on serologic testing for antibodies to borrelia burgdorferi Before cdc will recommend new tests, they must be cleared by the food and drug administration (fda). The test is a pass/fail test that determines whether you can detect a test agent, such as through taste, smell, or an involuntary cough Niosh does not endorse or recommend the use of the irritant smoke fit test. Placing test strips on a moist or newly cleaned surface may damage the strip and cause incorrect results Check and record temperatures of the testing, reagent, and test kit storage areas See appendix b for examples of daily temperature logs Check inventory regularly to ensure you have enough reagents, test kits, and supplies for testing. The tb skin test (also known as the mantoux tuberculin skin test or tst) is one method of determining whether a person is infected with tb bacteria Reliable administration and reading of the tb skin test requires standardization of procedures, training, supervision, and practice. Tb screening for health care personnel includes a risk assessment, symptom evaluation, and tb test. For more details on interpreting tb skin test results, please visit clinical testing guidance for tuberculosis Tb skin results should only be read by a trained health care professional Consult with your state and local public health authorities to determine who is authorized to place and read tb skin tests in your state. As with antibody tests for other infectious diseases, the accuracy of these tests depends upon how long you've been infected