医疗器械制造商应建立并维护流程以确保其所采购或者接收的产品或服务满足其规格要求。
Manufacturers shall establish and maintain procedures to ensure their purchased and otherwise received products and services conform to their specified requirements.
最后，讨论了综合双侧规格限情形的接收准则及图解法。
Finally, the acceptability criterion and its graphical method for the case with combined double specification limits are discussed.
如果验货时发现已接收的货物中有部分与需方所规定的规格不符，需方有权取消任何为交付货物的定单。
If inspection discloses that part of the goods received are not in accordance with Buyer's specifications, Buyer shall have the right to cancel any unshipped portion of the order.
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