§ 1.70 Scope.

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Title 21—Food and Drugs > CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES > SUBCHAPTER A—GENERAL > PART 1—GENERAL ENFORCEMENT REGULATIONS > Subpart D—Electronic Import Entries

This text was captured on Sep 22, 2026. It is a snapshot, not a live feed, so check the official code before relying on it.

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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.

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