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§113.83 修订加热杀菌工艺规程(Establishing scheduled processes)

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放大字体  缩小字体 2011-04-18 01:13:37  来源:GPO  浏览次数:3455
核心提示:低酸性食品的加热杀菌工艺规程必须由符合下列条件的合格人员制定,具有关于密封容器中低酸性食品加热杀菌要求的专门知识并能熟练迅速作出有关判断。在制定工艺规程时要充分考虑到商业性生产中遇到的方式、范围等的各种变化。该修订对上述的范围进行了进一步的解释。
发布单位
FDA
FDA
发布文号 76 FR 11922
发布日期 2011-03-03 生效日期 2012-03-05
有效性状态 废止日期 暂无
备注 低酸性食品的加热杀菌工艺规程必须由符合下列条件的合格人员制定,具有关于密封容器中低酸性食品加热杀菌要求的专门知识并能熟练迅速作出有关判断。在制定工艺规程时要充分考虑到商业性生产中遇到的方式、范围等的各种变化。该修订对上述的范围进行了进一步的解释。

  § 113.83   Establishing scheduled processes.

  Scheduled processes for low-acid foods shall be established by qualified persons having expert knowledge of thermal processing requirements for low-acid foods in hermetically sealed containers and having adequate facilities for making such determinations. The type, range, and combination of variations encountered in commercial production shall be adequately provided for in establishing the scheduled process. Variations include those that occur due to seasonal or growing fluctuations, variety differences, supplier processes, reprocessing, and mixing a batch of processed product with the same unprocessed product before it is processed. Critical factors, e.g., minimum headspace, consistency, maximum fill-in or drained weight, aw, etc., that may affect the scheduled process, shall be specified in the scheduled process. Acceptable scientific methods of establishing heat sterilization processes shall include, when necessary, but shall not be limited to, the use of microbial thermal death time data, process calculations based on product heat penetration data, and inoculated packs. Calculation shall be performed according to procedures recognized by competent processing authorities. If incubation tests are necessary for process confirmation, they shall include containers from test trials and from actual commercial production runs during the period of instituting the process. The incubation tests for confirmation of the scheduled processes should include the containers from the test trials and a number of containers from each of four or more actual commercial production runs. The number of containers from actual commercial production runs should be determined on the basis of recognized scientific methods to be of a size sufficient to ensure the adequacy of the process. Complete records covering all aspects of the establishment of the process and associated incubation tests shall be prepared and shall be permanently retained by the person or organization making the determination.

  更多关于美国FDA酸化食品HACCP法规,请详见美国FDA酸化食品HACCP法规第113和114部分汇总

 地区: 美国 
 标签: 酸性 杀菌 
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