Code of Federal Regulations > Title 21 > Chapter I > Part 1 > Subpart D - Subpart D—Electronic Import Entries

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Regulations last checked for updates: May 14, 2025

Title 21 - Food and Drugs last revised: May 12, 2025

All TitlesTitle 21Chapter IPart 1Subpart D - Subpart D—Electronic Import Entries

§ 1.70 - Scope.

§ 1.71 - Definitions.

§ 1.72 - Data elements that must be submitted in ACE for articles regulated by FDA.

§ 1.73 - Food.

§ 1.74 - Human drugs.

§ 1.75 - Animal drugs and veterinary devices.

§ 1.76 - Medical devices.

§ 1.77 - Radiation-emitting electronic products.

§ 1.78 - Biological products, HCT/Ps, and related drugs and medical devices.

§ 1.79 - Tobacco products.

§ 1.80 - Cosmetics.

§ 1.81 - Rejection of entry filing.

authority: 15 U.S.C. 1333,1453,1454,1455,4402; 19 U.S.C. 1490,1491; 21 U.S.C. 321,331,332,333,334,335a,342,343,350c,350d,350j,352,355,360b,360ccc,360ccc-1,360ccc-2,362,371,374,381,382,384a,387,387a,387c,393,and; 42 U.S.C. 216,241,243,262,264,271

source: 42 FR 15553, Mar. 22, 1977, unless otherwise noted.

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