未经检验合格的产品应放置在待检区，并挂待检牌，化验合格后才能转至合格成品区，挂合格检验牌。
Products not inspected shall be put in area to be inspected and carry tablet "to be inspected" and be transferred to area of qualified product and carry "qualified" tablet if tested qualified.
分析了零件模糊合格事件、零件模糊不合格事件、零件可修复模糊不合格事件和零件不可修复模糊不合格事件之间的关系。
The relations among the fuzzy qualified event, the fuzzy unqualified event, the mendable fuzzy unqualified event and the non-mendable fuzzy unqualified event of the parts are analyzed.
每次开机后，须先测试标准漏孔，然后测试不合格蒸发器样品应为不合格，测试合格样品应为合格（蒸发。器样品每月更换新的。）即校验仪器工作正常后，才能测试蒸发器。
Notice: Once begin the operation, standard leakage devices must be tested, then check the failed evaporator samples as "Fail" and passed evaporator samples as "Pass".
片剂说明书合格率为86.6%，胶囊剂说明书合格率为78.5%，外用制剂合格率为85.7%，液体制剂合格率为75%，注射剂合格率为75%。
Results: The qualification rate of tablets, capsules, external preparation, liquid preparation and injectable preparation were 86.6%, 78.5%, 85.7%, 75% and 75% respectively.
结果水疗室各项生物学指标均达标，总合格率为98.61%，物体表面合格率97.22%，医务人员手合格率98.61%，紫外线强度及室内空气合格率100.00%，消毒液合格率为97.22%。
RESULTS the total qualified rate was 98.61% and that of the object surface was 97.22%, of staff's hands was 98.61%, of UV intensity and indoor air was 100% and of the using disinfectant was 97.22%.
室内空气合格率为52.94%，物体表面合格率为86.3%，使用中消毒液合格率为94.57%。无菌器械和压力蒸汽灭菌器检测合格率分别为81.88%和76.92%。
The eligible rates of indoor air, surfaces, disinfection solution in use, sterile instruments and autoclave were 52.94%, 86.3%, (94.57%), 81.88% and 76.92% respectively.
室内空气合格率为52.94%，物体表面合格率为86.3%，使用中消毒液合格率为94.57%。无菌器械和压力蒸汽灭菌器检测合格率分别为81.88%和76.92%。
The eligible rates of indoor air, surfaces, disinfection solution in use, sterile instruments and autoclave were 52.94%, 86.3%, (94.57%), 81.88% and 76.92% respectively.
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