eCFR Reference Browser

---

title: "21 CFR §1.70"

source: "https://www.ecfr.gov/current/title-21/section-1.70"

title_number: "21"

volume_number: "1"

chapter_number: "Unknown"

subchapter_code: "A"

subchapter_subject: "GENERAL"

part_code: "1"

part_subject: "GENERAL ENFORCEMENT REGULATIONS"

subpart_code: "D"

subpart_subject: "Electronic Import Entries"

section_number: "1.70"

section_subject: "Scope."

cfr_reference: "21 CFR 1.70"

title_name: "Title 21"

title_subject: "Food and Drugs"

parts_covered: "Parts 1 to 99"

revised_date: "Revised as of April 1, 2019"

publication_date: "As of April 1, 2019"

contains_description: "Containing a codification of documents of general applicability and future effect"

publication_info: "Published by the Office of the Federal Register National Archives and Records Administration as a Special Edition of the Federal Register"

---

This subpart specifies the data elements that are required by the Food and Drug Administration (FDA) to be included in an electronic import entry submitted in the Automated Commercial Environment (ACE) system or any other U.S. Customs and Border Protection (CBP)-authorized electronic data interchange (EDI) system, which contains an article that is being imported or offered for import into the United States and that is regulated by FDA.

§1.70 - Scope.