6.7.7检验不合格之处理6.7.7.1仪器校验不合格或在有效期限内故

6.7.7 unqualified of handling <br>6.7.7.1 instrument calibration failure or malfunction within the validity period shall be labeled as "suspended" tab, and arrange for repair. At the same time, the judge failed to retain records in accordance with the "records management program." <br>6.7.7.2 When they find the instrument calibration failure, the unit must be in conjunction with the school instrument by the use of units, quality assurance units and R & D units (if necessary), the effectiveness of past test results and the test results, to be assessed, continuous tracking three batches , if abnormal, the product has been traced back to pass up. At the same time, the relevant records to fill in the "Instrument Calibration Failure Assessment Form." <br>Instrument calibration failure confirmation process assessment evaluation table:

6.7.7 Handling of non-conformity 6.7.7.1 If the instrument is unqualified or fails within the effective period, it shall be labeled "Suspended" and repair arranged.<br>At the same time, records of non-conformity will be retained in accordance with the Records Management Procedure. 6.7.7.2 When the instrument is found to be ineffective, it must be evaluated by the unit of the user in conjunction with the equipment school unit, the quality assurance unit and the research and development unit (if necessary), to evaluate the validity of the past inspection results and test results, and to track three batches of products in succession, if there are anomalies, all the way back to the product qualified.<br>At the same time, the relevant records are filled in the Instrument Correction Failure Assessment Form. Instrument verification failure assessment form evaluation confirmation process:

6.7.7 handling of unqualified inspection<br>6.7.7.1 if the instrument fails to pass the calibration or fails within the validity period, the label of "suspension of use" shall be pasted and maintenance shall be arranged. At the same time, the unqualified records shall be kept according to the record management procedure.<br>6.7.7.2 in case of failure of instrument calibration, the user, together with instrument calibration unit, quality assurance unit and R & D unit (if necessary), must evaluate the validity of past inspection results and test results, and track three batches of products continuously. If there is any abnormality, it shall be traced back to the qualified products. At the same time, the relevant records shall be filled in the "instrument calibration failure evaluation form".<br>Assessment and confirmation process of instrument calibration failure assessment form:<br>