控制約定的材料  Are suspect and identified non-conforming materials, componentsand products clearly identified and segregated at all stages to preventfurther use?

　　工廠(chǎng)對于被懷疑的或鑒別為不合格的物料、零配件、產(chǎn)品，在每個(gè)生產(chǎn)環(huán)節是否有清晰的標識和有效的分隔，以防止進(jìn)一步使用？

　　Look for areas in the factory that are used only for segregated, non-conforming- rejected rawmaterial and product. These areas must be identified by labels, writing, etc. on the walls. Productcan be finished or in-process. Non-Conforming product must be clearly identified by specialcolored tags or labels and/or placed in containers that are clearly identified or differentiated fromnormal production.

　　核對工廠(chǎng)的不合格原材料及不合格產(chǎn)品區域是否專(zhuān)門(mén)用來(lái)分隔瑕疵品。該區域必須用標簽或其他書(shū)寫(xiě)標識等張貼在墻上。

　　不合格品可能來(lái)自于成品及半成品。

　　不合格品必須用特殊顏色的標貼或者吊牌加以區分，或者存放于有明顯標識的、非正常生產(chǎn)的區域。

　　 控制約定的材料  Do records of non-conforming materials, components and productsexist?

　　工廠(chǎng)是否有不合格物料/零配件/產(chǎn)品的記錄？

　　Verify that records exist that non-conforming material/product is monitored prior to re-work ordestruction. Non-conforming can be product that has failed inspection, contains defects, does notmeet specs, etc. The records must include the following:

　　A. QuantityB. Type of non-conformance or defectC. Source or point of where identified as being non-conformingD. Current statusE. Resulting dispositionF. Person(s) making the dispositionG. If reworked, evidence or documentation of reinspectionH. Traceability to corrective action (remedial action) records.

　　I. Traceability to engineering change requests and product specification changes.

　　核對工廠(chǎng)的不合格物料、產(chǎn)品在返工或者銷(xiāo)毀之前有相應的檢驗記錄。不合格產(chǎn)品有可能是由于驗貨有問(wèn)題，有瑕疵，與客戶(hù)工藝要求不符等。不合格產(chǎn)品檢驗記錄必須包含以下內容：

　　A. 數量B. 疵點(diǎn)類(lèi)型C. 次品來(lái)源或者瑕疵部位D. 現在的情況E. 處置結果F. 負責人G. 如需返工,重新檢驗的記錄H. 可追溯的糾正和預防措施記錄I . 可追溯的生產(chǎn)程序改變的申請記錄和最新工藝單 Control of Non-Conforming MaterialsIs there evidence to prove that non-conforming materials and theirpackaging are handled and disposed of according to customerrequirements and/or legal requirements?

　　工廠(chǎng)是否有相關(guān)記錄，證明不合格物料、產(chǎn)品以及零售包裝根據客戶(hù)要求或者法律法規要求進(jìn)行了適當的處置？

　　Review documentation to verify that client requirements are being followed by the factory indisposing of second quality, overruns and cancellations, etc. If factory is working for Target must beconsistent with Target's policy posted on POL > Brand Protection.

　　核對工廠(chǎng)的記錄來(lái)驗證工廠(chǎng)在處理二等品、多做的產(chǎn)品和因訂單取消產(chǎn)生的多余產(chǎn)品是遵循了客戶(hù)的相關(guān)要求。

　　如果工廠(chǎng)生產(chǎn)Target自主品牌產(chǎn)品，應該遵守Target在www.partnersonline.com網(wǎng)站 Brand Protection 項下公布的不合格產(chǎn)品處理規定。

　　 控制約定的材料  Does the non-conforming material system allow for operators toidentify and flag defective goods on the line?

　　工廠(chǎng)的不合格產(chǎn)品管控系統是否允許操作人員在生產(chǎn)線(xiàn)上標示瑕疵品？

　　Check during your tour if operators are separating defective units and identifying them. Usuallystickers are used or the units are placed in special designated containers.

　　在參觀(guān)生產(chǎn)現場(chǎng)的過(guò)程中，核實(shí)工廠(chǎng)的操作人員是否有效的將不合格產(chǎn)品分隔并標注。

　　通常操作人員用瑕疵標貼做為標識，不合格產(chǎn)品存放在指定的區域。

　　 控制約定的材料  Does the factory have procedures to ensure that customers arenotified immediately on issues of product safety or legality (noncompliancewith any rule, ban, standard and regulation)?

　　工廠(chǎng)是否有程序文件規定，當發(fā)現產(chǎn)品存在安全或違反法律法規（與任何法規、禁令、客戶(hù)標準及常規要求不符）時(shí)，必須及時(shí)通知客戶(hù)？

　　Review SOP documentation for direction of notifying customers when product has been identifiedas being not in compliance with any rule, ban, standard or regulation and has potentially exited thefactory. Look for evidence (records) of this happening. Customer must be notified if any noncomformingproduct potentially exited the factory.

　　核對工廠(chǎng)的標準操作流程文件并驗證，當產(chǎn)品存在與任何法規、禁令、客戶(hù)標準及常規要求不符時(shí)或者存在潛在不符點(diǎn)時(shí)，及時(shí)通知客戶(hù)。

　　核對工廠(chǎng)處理此類(lèi)事件的記錄，證明客戶(hù)得到了工廠(chǎng)的及時(shí)通知。

　　 控制約定的材料  Are the non-conforming procedures understood by the factorypersonnel and implemented effectively?

　　工廠(chǎng)的員工是否理解及有效地執行對于不合格產(chǎn)品的處理程序？

　　When out on the factory floor interview workers to determine if they understand the factory's SOPon how to identify & handle non-conforming materials/products. Look for evidence of the factorySOP being followed.

　　在參觀(guān)工廠(chǎng)車(chē)間時(shí)，同工人簡(jiǎn)明面談以確定他們是否了解如何識別和處理不合格物料、產(chǎn)品的標準操作程序。

　　核對工廠(chǎng)的相關(guān)記錄加以驗證。

　　 糾正措施/補救行動(dòng)計劃
  Does the factory have an effective documented corrective actionsystem for the timely investigation & resolution of nonconformitiesthat may affect meeting safety, regulatory and quality requirementsof the product?

　　工廠(chǎng)是否有內部糾錯系統，分析不合格產(chǎn)品的產(chǎn)生原因和制定相應解決方案來(lái)確保產(chǎn)品符合安全，法律法規和產(chǎn)品質(zhì)量要求？

　　Verify the factory has a written SOP that addresses taking corrective action when productnonconformance's related to safety, legality or quality are identified. Ask for and review records ofcorrective action to determine if the system is being used and working properly.

　　核對工廠(chǎng)的糾錯標準操作程序文件。

　　它應該清晰描述，當面臨產(chǎn)品不符合安全，法律法規和質(zhì)量要求時(shí)，應該立即啟動(dòng)糾錯系統。

　　核對工廠(chǎng)的糾錯記錄，以確定此系統正在使用和有效的運行。

　　 糾正措施/補救行動(dòng)計劃
  Does the corrective action system meet Target minimumrequirements?

　　工廠(chǎng)的糾錯系統是否符合Target的最低要求？

　　All of the following minimum Target requirements for corrective action system must be met:

　　A. Problem statementB. Root cause statementC. Corrective action statement along with date of implementation.

　　D. Appropriate staff member is identified for the responsibility and accountability of the correctiveaction (remedial action).

　　E. Traceability to the occurrence that triggered the initiation of the corrective action (remedialaction) such as test results, inspection results, nonconforming material/product dispositions, etc.

　　F. If applicable, traceability to engineering change requests, specification changes andrecertification testing.

　　G. Follow-up for determination of effectiveness of the corrective action (remedial action).

　　Target對于糾錯系統的最低要求包含：

　　A. 問(wèn)題的描述B. 根本原因分析C. 改進(jìn)方案及執行日期.

　　D. 糾正/補救措施相關(guān)人員的職責和責任E. 發(fā)現問(wèn)題的源頭：

　　如測試結果,檢驗結果,不合格物料/產(chǎn)品的處置等F. 如果適用性，可追溯至：

　　相關(guān)技術(shù)變更，工藝修改和重新認證測試等G. 后續跟蹤對于執行糾正/補救措施有效性的鑒定評估 Corrective Action/Remedial Action PlansIs Data collected, such as but not limited to: product testing results,product inspection results, customer complaints and recalls used toinitiate corrective action/remedial action?

　　工廠(chǎng)的糾錯系統是否收集相關(guān)數據?數據包含但不僅限于：

　　-產(chǎn)品的測試結果-產(chǎn)品檢驗結果-客戶(hù)投訴和召回而啟動(dòng)糾正、補救措施Review the SOP & corrective action records to verify they are initiated by product test failures,inspection failures and customer complaints. Review product test failures, inspection failures andcustomer complaints to see if corrective actions were initiated.

　　核對工廠(chǎng)的糾錯標準操作流程文件及糾錯記錄。

　　驗證糾錯行動(dòng)原因是否由測試失敗、檢驗不合格和客戶(hù)投訴而采取的。

　　核對產(chǎn)品測試、檢驗不合格和客戶(hù)投訴，驗證是否啟動(dòng)了糾錯系統。

　　 糾正措施/補救行動(dòng)計劃
   Do individual corrective action/remedial action records exist? 工廠(chǎng)是否有單獨的糾正、補救措施記錄？

　　Ask for the factory's corrective action records. Verify the factory is keeping these records and thatthese records are recording the minimum Target requirements for corrective action information aslisted above.

　　核對工廠(chǎng)的糾錯記錄。

　　驗證工廠(chǎng)妥善保管相應糾錯記錄并且列出的糾正措施符合Target對于糾錯系統的最低要求。

　　 糾正措施/補救行動(dòng)計劃
  Are effective corrective actions/remedial actions taken andcompleted within an appropriate and defined time period?

　　工廠(chǎng)的糾正、補救措施是否在適當的和規定的時(shí)間內完成？

　　Review corrective action records. Verify the corrective actions are appropriate for the statedproblem. Verify corrective actions are being implemented timely and closed out within the timeframes specified in their corrective action SOP.

　　核對工廠(chǎng)的糾錯記錄。

　　驗證糾正措施是否適用于發(fā)現的問(wèn)題。

　　驗證糾正措施實(shí)施的時(shí)效性符合糾錯標準操作程序的規定。