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FDA Application of the Foreign Supplier Verification Program Regulation to Importers of Grain Raw Agricultural Commodities

蒋千琴 10/19/2021 浏览 230 FDA United States

标准简介

Application of the Foreign Supplier Verification Program Regulation to Importers of Grain Raw Agricultural Commodities[附网盘链接]是Food And Drug Administration发布的FDA标准，适用于United States。

标准截图

Application of the Foreign Supplier Verification Program Regulation to Importers of Grain Raw Agricultural Commodities[附网盘链接]
Application of the Foreign Supplier Verification Program Regulation to Importers of Grain Raw Agricultural Commodities[附网盘链接](截图)

 

标准文档说明

标准文档类型为Application of the Foreign Supplier Verification Program Regulation to Importers of Grain Raw Agricultural Commodities[附网盘链接]高清PDF版本（文字版），标准文档内可进行搜索，可以复制原文，可粘贴。

标准部分原文

Contains Nonbinding Recommendations Application of the Foreign Supplier Verification Program Regulation to Importers of Grain Raw Agricultural Commodities: Guidance for Industry This guidance represents the current thinking of the Food and Drug Administration (FDA, the Agency, or we) on this topic. It does not establish any rights for any person and is not binding on FDA or the public. You can use an alternative approach if it satisfies the requirements of the applicable statutes and regulations. To discuss an alternative approach, contact the FDA staff responsible for this guidance as listed on the title page. I. Introduction The purpose of this document is to state the Food and Drug Administration’s (FDA’s) intent to exercise enforcement discretion regarding application of the regulation on foreign supplier verification programs (FSVPs) to importers of grains imported into the United States as raw agricultural commodities (RACs). For the reasons stated below, we intend to exercise enforcement discretion with respect to the FSVP regulation for importers of grain RACs that are solely engaged in the storage of grain intended for further distribution or processing and grain importers that do not take physical possession of the grain they import but instead arrange for the delivery of the grain to others for storage, packing, or manufacturing/processing (such as certain commodity brokers with respect to the FSVP regulation). We are issuing this guidance consistent with our good guidance practices (GGP) regulation (21 CFR 10.115). This guidance is immediately effective because FDA has determined that prior public participation is not feasible or appropriate (21 CFR 10.115(g)(2)). FDA’s guidance documents, including this guidance, do not establish legally enforceable responsibilities. Instead, guidances describe the Agency’s current thinking on a topic and should be viewed only as recommendations, unless specific regulatory or statutory requirements are cited. The use of the word should in Agency guidances means that something is suggested or recommended, but not required. This guidance provides information to facilitate understanding of the applicability of the FSVP requirements to the importation of grain RACs. The pronouns “I,” “me,” and “you” are used in this guidance to refer to the importer. “Agency” and the pronouns “we” and “our” are used to refer to FDA.

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