食品伙伴網(wǎng)訊   據(jù)美國(guó)FDA消息，10月5日美國(guó)FDA發(fā)布通告稱，已經(jīng)完成對(duì)填制新流程表格草案的評(píng)議審核，要求酸化和低酸罐頭食品生產(chǎn)廠應(yīng)根據(jù)21CFR108.25（c）（2）和21CFR108.35（c）（2）向FDA提交相關(guān)新表格。新表格將代替FDA老的流程填制表格。新表格目前在FDA網(wǎng)站上提供，以方便生產(chǎn)廠使用。老表格也提供，但是，一旦FDA完成對(duì)21CFR第108章中法規(guī)的修改流程之后，將不再提供老表格。

酸化和低酸罐頭食品生產(chǎn)廠商可根據(jù)生產(chǎn)工藝選擇合適的表格，共有四類。

    部分原文報(bào)道如下：

    The Food and Drug Administration (FDA) has completed its review of public comments received on drafts of new process filing forms that acidified and low-acid canned food manufacturers will be required to file with the agency under 21 CFR 108.25(c)(2) and 21 CFR 108.35(c)(2). FDA has made changes to the draft forms and instructions wher appropriate, and has made the revised forms and instructions available to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act (PRA).

    原文鏈接：http://www.fda.gov/Food/NewsEvents/ConstituentUpdates/ucm465585.htm