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It means the record did not give FDA enough reliable, form-specific information to resolve the question under the criteria it was applying

doi: 10.1111/dom.15896 78 HuangYNLiaoWLHuangJYLinYJYangSFHuangCCet al

Regarding safety, the majority of reported adverse events were mild to moderate, ranging from 88% to 96%, depending on the specific study group

Under sunny conditions, photons are highly abundant, but closing the stomata limits gas exchange and hence the availability of the electron acceptors ADP + and NADP + from the CalvinBenson cycle

Dunne, A

These may be more accurate in some cases, but the process is more complicated