Based on the initial escalation analysis, it was suggested to issue an rma for the sensor 240552 as the root cause for noise in the glucose readings could not be confirmed.The rma was authorized to bring back the sensor for further investigation.Upon receiving the rma, the sensor was tested in-house, and the review of qc did not reveal any malfunction of the sensor.As part of resolution, a rma was authorized to offer the user, a sensor replacement.H3.Device evaluated by manufacturer?yes.H6.Type of investigation updated to 10.H6.Investigation findings updated to 213.H6.Investigation conclusions updated to 67.
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