TS16949 system in the process of establishing and implementing common problems 03 7.2 prone to Question 1, there is no contract procedures; 2, the program does not fully or misinterpreted (often deliberately), or contradict each other (such as: design, sales and production between); 3, record inadequate or non-existent; 4, the customer does not intervene; 5, no documented procedures to process orders; 6, feedback customer experience is not sufficient; 7, do not consider delivery and post-delivery activities requirements. 7.3 Chapter prone to question 1, the design responsibility / privilege / interface is not specified in writing or execution; 2, the team did not coordinate, particularly between the product liability and process responsibility; 3, drawing no control Hebei TS16949 certification, because: Tolerance unreasonable; drawings are not examined or verified; drawings unauthorized, or not use the change control system; drawings appeared subjective description. 4, the lack of practical design review, for example, a system of personal (people who voluntarily choose to partner) operations; 5, a system that appears in the written document TS16949 certification costs, but do not use; 6, the specified tolerance can not be achieved (eg: Missing production intervention); 7, prototype sample does not meet the key test items; 8, started asking if the user manual is designed almost complete; 9, measuring and test equipment used in experimental work not calibrated; 10, sampling system is defective or not the consent of the client. ISO / TS16949: 2009 certification 04 Organisations who supply service parts can achieve certification if they manufacture parts to OEM specification, and those parts are distributed via the OEM official dealer network organization made of OEM parts for maintenance (including repair parts) applications purchase or published, according to OEM specification parts manufactured Huanghua TS16949 certification, this technical specification can be certified. Organisations who manufacture aftermarket parts, which are not to OEM specification, or not distributed through the OEM network, can not achieve certification tissue repair and not by the original manufacturer specifications by the original distribution channel or who can not be authenticated. TS16949 internal audit skills: syllogism nonconformance report (syllogism): 1, not satisfied; 2, requirements, or the requirements of the specific reference; 3, in line with statements of support does not prove incompatible with objective evidence of reasonable classification. Note: one does not meet can cover more than one "should of" requirement.