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Positive recall is a term used in quality systems, most notably ISO9000.It is part of receiving inspection procedures. [1] It defines the concept that if a producer or manufacturer receives a product or process that requires inspection and it wishes to postpone the inspection process, it must have a system in place that will ensure that the postponed inspection process will take place at some ...
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[2] [3] During the development of the 9TXX, GM received 60 new patents while building 800 prototypes. [4] It was developed from the 6T41 (Gen 3) [5] and designed to occupy approximately the same volume as that prior six-speed automatic and retain that transmission's on-axis design, which aligns all the planetary gears with the crankshaft.
A Publicly Available Specification or PAS is a standardization document that closely resembles a formal standard in structure and format but which has a different development model. [1] The objective of a Publicly Available Specification is to speed up standardization. PASs are often produced in response to an urgent market need. [2]
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FDA's role under the guidelines is to monitor company recalls and assess the adequacy of a firm's action. After a recall is completed, FDA makes sure that the product is destroyed or suitably reconditioned and investigates why the product was defective. Generally, FDA accepts reports and other necessary recall information submitted by e-mail.
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The first version of the standard was published in 2003, and it was revised in 2007 to align more closely to ISO/IEC 17025. [1] A third edition of the standard was published in 2012, which revised the layout again and added a section on laboratory information management.