当判定需要发出纠正预防措施报告时，品质部须对纠正及纠正措施的完成情况进

When it is judged necessary to issue corrective precautions report, the Department of quality required for the completion of correction and corrective actions to track, verify and complete the track record. <br>5.3.5 Complaints closed: <br>1) when the sales process of communication with customers complaints accepted to close the <br>related documents Sales of communication with customers, record passed to the Department of Quality <br>5.3.6 may be any product label or package failed meet their specifications complaints shall be subject to review, evaluation and investigation, unless due to a similar complaint was investigated. <br>5.4 customer complaints commitments <br>related departments to deal with the results of customer complaints should take timely and effective measures to prevent similar incidents from happening again. <br>5.5 Sales records should be kept handle customer complaints and submit a management review, retention requirements specified by the "quality records management program" implementation.

When a corrective action report is determined to be issued, the Quality Department shall track the completion of corrective and corrective actions and complete the tracking verification record.<br>5.3.5 Complaint systowas:<br>1) Close when the sales department communicates with the customer the acceptance of the handling of the complaint<br>The relevant documents and records communicated by the sales department to the customer are passed to the quality department<br>5.3.6 Any complaint that the product, label or packaging may have failed to meet its specifications shall be reviewed, evaluated and investigated, unless a similar complaint has been investigated. 5.<br>4 Promise of customer complaints<br>Relevant departments should take timely and effective measures to prevent similar incidents from happening again. 5. 5 Sales department should keep the customer complaint handling record and submit to the management review, the preservation requirements in accordance with the Quality Records Management Procedure.

When it is determined that a corrective and preventive action report needs to be issued, the quality department shall track the completion of the corrective and corrective actions, and complete the tracking and verification records.<br>5.3.5 closure of complaints:<br>1) it can be closed when the sales department communicates with the customer and accepts the handling of the complaint.<br>Relevant documents and records of communication between the sales department and customers shall be transferred to the quality department.<br>5.3.6 any complaint that the product, label or package fails to meet the specification shall be reviewed, evaluated and investigated, unless it has been investigated due to a similar complaint.<br>5.4 commitment of customer complaints<br>Relevant departments shall take timely and effective measures for the handling results of customer complaints to prevent similar incidents from happening again.<br>5.5 the sales department shall keep the handling records of customer complaints and submit them to the management review. The retention requirements shall be in accordance with the quality record management procedure.<br>