Due to the particularity of the sample itself, it is necessary to clean the instrument to reduce the requirement of standard 5. The probability of such events is that the deviation is caused by the particularity of the sample itself and the pollution of the digestion tank. The original test data is invalid and retained, which has no impact on the product quality. Among them, the retest results of standard 5 in the retest test of 2090011n210102 stock solution reached the acceptance standard, and the retest data were accurate and reliable, which could be used for the release results. However, the contaminated digestion tank was used for 2090011n210102 batch of samples, which affected the accuracy of the test results, and the test results were not credible, so it was necessary to retest the batch of samples. It is not clearly stated in the method of the product that the instrument injection system needs to be cleaned before standard 5 retest, and the detection method of [palladium] in h0-am-20008-01 moxifloxacin hydrochloride physical and chemical test method 03 needs to be refined. There are some defects in the management of the digestion tank that are clearly polluted, so it needs to be stored separately and clearly marked to avoid mixed use.<br>
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