FCCA Quality System Audit Outline

FCCA Quality System Audit Outline

4.0 Process and Production Control過程和生產(chǎn)控制

4.0.1 Does factory have work area only for Product Development? 工廠是否有產(chǎn)品開發(fā)工作區(qū)？

4.0.2 Does factory PD study and apply product safety features, evaluates patterns, moulds and samples during product design and development? 在產(chǎn)品設(shè)計和開發(fā)工廠產(chǎn)品開發(fā)的研究與應(yīng)用是否有產(chǎn)品安全功能、評估模式、模具和樣品？

4.0.3 Does Product development includes packaging design and tests that conforms to industry standard (ISTA) 產(chǎn)品開發(fā)包括包裝設(shè)計和測試以確保符合行業(yè)標(biāo)準(zhǔn)(ISTA)。

4.0.4 Does factory PD perform assembly time-study on product and develop easy ways to use for consumer benefit? 工廠產(chǎn)品開發(fā)在產(chǎn)品執(zhí)行組裝時間研究，產(chǎn)品開發(fā)和簡便的方法使用的消費者受益呢？

4.0.5 Factory has documented Production procedures at each stage of operation. 工廠有每一個階段的運作生產(chǎn)程序文件。

4.0.6 Factory has documented Quality procedures at each stage of operation. 工廠有每一個階段的運作質(zhì)量程序文件。

4.0.7 Does factory conduct Pre-production meeting prior to start of production?工廠是否實施進行生產(chǎn)前的預(yù)產(chǎn)會議？

4.0.8 Are production and quality supervisors present during Pre-production meeting?目前在預(yù)產(chǎn)會議有生產(chǎn)和質(zhì)量主管？

4.0.9 (Critical) Are critical quality and safety checks reviewed, identified, and actions for improvement documented during Pre-production meeting? (重要)是至關(guān)重要的質(zhì)量和安全檢查、審查，確定，并采取行動加以改進記錄在預(yù)產(chǎn)會議？

4.0.10 Does factory conduct “pilot-run”, review product quality against specification sheet and document results with corrective actions prior to production?工廠是否進行“試運行”，檢討對產(chǎn)品質(zhì)量的規(guī)格表和文件在糾正行動之前生產(chǎn)？

4.0.11 Is quality of item acceptable on current production? (Check 3 or 4 completed products from production floor). 質(zhì)量是可以接受的項目就目前的生產(chǎn)呢？(從生產(chǎn)區(qū)檢查3或4個成品)。

4.0.12 Was in house lab-testing performed on current production? (Request for test copies)內(nèi)部實驗室測試是否實施當(dāng)前生產(chǎn)測試？(要求測試的副本)

4.0.13 Does factory QC compare first piece samples with approval sample and specification sheet? 工廠QC是否比較首件樣品抽樣檢驗和批準(zhǔn)的規(guī)格表？

4.0.14 Are there adequate approved samples, first piece samples, reference samples and work instructions to provide workers with proper guidelines? 是否有足夠的核準(zhǔn)樣品、首件樣品、參考樣品和為工人提供適當(dāng)?shù)淖鳂I(yè)指導(dǎo)書？

4.0.15 Does factory use defective/ reject samples to demonstrate examples of common defects?

工廠使用有缺陷的/不合格樣品是否普遍例子？

4.0.16 (Critical) Does Quality Control have authority to stop production if quality of products did not meet specification? (重要)如果產(chǎn)品質(zhì)量不符合規(guī)格質(zhì)量控制是否有權(quán)停止生產(chǎn)？

4.0.17 In-line inspections (IPQC) are performed by QC at every operation process. 在巡檢(IPQC)所執(zhí)行品管在每一個操作過程。

4.0.18 Does factory use statistical process control (SPC for quality)?工廠使用統(tǒng)計過程控制?(質(zhì)量統(tǒng)計分析)

4.0.19 Factory QC inspects per standard AQL or as per industry standards.工廠品管檢驗按照標(biāo)準(zhǔn)AQL或按照工業(yè)標(biāo)準(zhǔn).

4.0.20 Factory performs 100% functionality check on final products?工廠最終產(chǎn)品實施100%功能性確認(rèn)?

4.0.21 Does factory use corrective actions and root cause analysis methods? (Please provide examples)工廠是否使用的糾正措施和根本原因分析方法呢？(請?zhí)峁├?

4.0.22 Does factory have guidelines in place to ensure packaging is correct for product? 工廠是否有指南以適當(dāng)確保包裝是正確的產(chǎn)品？

4.0.23 Does packing area have enough space to perform packing functions properly? Is it clean and organized? 包裝區(qū)是否有足夠的空間用來履行包裝職能？它是清潔和有組織的？

4.0.24 Packed cartons are stored in enclosed area not exposed to sunshine and wet weather. 包裝紙箱都儲存在封閉區(qū)域內(nèi)沒有暴露于陽光和潮濕天氣。

4.0.25 Does factory track and document on-time ship performance?工廠是否有跟蹤和文件準(zhǔn)時出貨職能？

4.1 Suppliers and Sub-contractors供應(yīng)商和分包商

4.1.1 Does factory have a documented supplier selection and approval process?工廠是否有供應(yīng)商選擇和批準(zhǔn)過程文件?

4.1.2 Does factory track, evaluate and document material’s supplier reliability (performance)?工廠是否跟蹤、評價和文件物料供應(yīng)商的可*性(效能) ？

4.1.3 Does factory have an established, documented quality procedure and does factory evaluate, monitor sub-contractor quality performance and reliability? 工廠是否有建立質(zhì)量記錄的程序和工廠評估、監(jiān)測分包商的質(zhì)量性能和可*性呢？

5.0 In-House Lab-Testing內(nèi)部實驗室-測試

5.0.1 Does factory perform in-house lab testing and are facilities appropriately equipped? 工廠是否執(zhí)行內(nèi)部實驗室測試和配備適當(dāng)設(shè)施？

5.0.2 All gauges and test equipments have valid calibrations.所有量規(guī)和測試設(shè)備有效校準(zhǔn)。

5.0.3 Testing manuals of various industry standards are available as reference.各種行業(yè)標(biāo)準(zhǔn)測試手冊是可作為參考。

5.0.4 In-house Lab Technicians are properly trained to perform testing functions. 在內(nèi)部實驗室的技術(shù)人員受過適當(dāng)訓(xùn)練的執(zhí)行測試功能。

6.0 Final inspection最終檢驗

6.0.1 Does factory QC performs final inspection and documents it?工廠QC是否執(zhí)行最終檢驗和文件？

6.0.2 An approved sample or reference sample with packing list and shipping marks are available as reference for factory QC. 已核準(zhǔn)的樣品或參考樣品與包裝清單和嘜頭，可作為工廠品管參考的。

6.0.3 (Critical) Failed inspections are properly corrected prior to final inspection by customer.

(重要的)失效檢驗得到適當(dāng)糾正在客戶最終檢驗。

6.0.4 Factory does not ship goods unless subjected to release procedures from customer.

工廠不出貨的貨物除非從客戶獲得豁免的程序。

7.0 People Resources and Training人力資源和培訓(xùn)

7.0.1 (Critical) Factory conducts, documents, maintains on-job training for all personnel, or conducts pre-hire testing of skilled workers prior to hiring. (重要)工廠進行、文件、保持對在職培訓(xùn)的所有人員或進行崗前技能培訓(xùn)。

7.0.2 Factory conducts and documents technical training programs for Electrical/ Mechanical Engineer, Machinist, QA Auditor and Lab Test Technician. 工廠進行和文件的技術(shù)培訓(xùn)計劃電動/機械工程師，機械師，質(zhì)量保證審計員和實驗室測試技術(shù)員。

7.0.3 Records of trainees and all regular personnel with corresponding performance records are kept and maintained. 記錄學(xué)員及所有工作人員定期與相應(yīng)的業(yè)績記錄，保存和維修保養(yǎng)。