# 21 CFR § 1.70: Scope

> Federal · Regulations · In force

URL: https://www.frixlaw.com/law-library/statutes/ecfr-21-1.70

## Section

- **Citation:** 21 CFR § 1.70
- **Heading:** Scope
- **Jurisdiction:** Federal
- **Kind:** Regulations
- **Status:** In force
- **Text as of:** September 22, 2026
- **Source:** Publisher's official text
- **Location:** 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

## Text

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.

## Nearby sections

- [21 CFR § 1.1 § 1.1 General.](https://www.frixlaw.com/law-library/statutes/ecfr-21-1.1.md)
- [21 CFR § 1.3 § 1.3 Definitions.](https://www.frixlaw.com/law-library/statutes/ecfr-21-1.3.md)
- [21 CFR § 1.4 § 1.4 Authority citations.](https://www.frixlaw.com/law-library/statutes/ecfr-21-1.4.md)
- [21 CFR § 1.20 § 1.20 Presence of mandatory label information.](https://www.frixlaw.com/law-library/statutes/ecfr-21-1.20.md)
- [21 CFR § 1.21 § 1.21 Failure to reveal material facts.](https://www.frixlaw.com/law-library/statutes/ecfr-21-1.21.md)
- [21 CFR § 1.23 § 1.23 Procedures for requesting variations and exemptions from required label statements.](https://www.frixlaw.com/law-library/statutes/ecfr-21-1.23.md)
- [21 CFR § 1.24 § 1.24 Exemptions from required label statements.](https://www.frixlaw.com/law-library/statutes/ecfr-21-1.24.md)
- [21 CFR § 1.70 § 1.70 Scope.](https://www.frixlaw.com/law-library/statutes/ecfr-21-1.70.md)
- [21 CFR § 1.71 § 1.71 Definitions.](https://www.frixlaw.com/law-library/statutes/ecfr-21-1.71.md)
- [21 CFR § 1.72 § 1.72 Data elements that must be submitted in ACE for articles regulated by FDA.](https://www.frixlaw.com/law-library/statutes/ecfr-21-1.72.md)
- [21 CFR § 1.73 § 1.73 Food.](https://www.frixlaw.com/law-library/statutes/ecfr-21-1.73.md)
- [21 CFR § 1.74 § 1.74 Human drugs.](https://www.frixlaw.com/law-library/statutes/ecfr-21-1.74.md)
- [21 CFR § 1.75 § 1.75 Animal drugs and veterinary devices.](https://www.frixlaw.com/law-library/statutes/ecfr-21-1.75.md)
- [21 CFR § 1.76 § 1.76 Medical devices.](https://www.frixlaw.com/law-library/statutes/ecfr-21-1.76.md)

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Source: Frix Law Library, https://www.frixlaw.com/law-library/statutes/ecfr-21-1.70. Check the current official text before relying on it. Not legal advice.