Title 21

PART 1 SUBPART D

Subpart D - Electronic Import Entries Source:81 FR 85870, Nov. 29, 2016, unless otherwise noted.

• 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, 350e, 350j, 350k, 352, 355, 360b, 360ccc, 360ccc-1, 360ccc-2, 362, 371, 373, 374, 379j-31, 381, 382, 384, 384a, 384b, 384d, 387, 387a, 387c, 393; 42 U.S.C. 216, 241, 243, 262, 264, 271; Pub. L. 107-188, 116 Stat. 594, 668-69; Pub. L. 111-353, 124 Stat. 3885, 3889.
• Source: 42 FR 15553, Mar. 22, 1977, unless otherwise noted.

21:1.0.1.1.1.4.32.1	SECTION 1.70	1.70 Scope.
21:1.0.1.1.1.4.32.2	SECTION 1.71	1.71 Definitions.
21:1.0.1.1.1.4.32.3	SECTION 1.72	1.72 Data elements that must be submitted in ACE for articles regulated by FDA.
21:1.0.1.1.1.4.32.4	SECTION 1.73	1.73 Food.
21:1.0.1.1.1.4.32.5	SECTION 1.74	1.74 Human drugs.
21:1.0.1.1.1.4.32.6	SECTION 1.75	1.75 Animal drugs.
21:1.0.1.1.1.4.32.7	SECTION 1.76	1.76 Medical devices.
21:1.0.1.1.1.4.32.8	SECTION 1.77	1.77 Radiation-emitting electronic products.
21:1.0.1.1.1.4.32.9	SECTION 1.78	1.78 Biological products, HCT/Ps, and related drugs and medical devices.
21:1.0.1.1.1.4.32.10	SECTION 1.79	1.79 Tobacco products.
21:1.0.1.1.1.4.32.11	SECTION 1.80	1.80 Cosmetics.
21:1.0.1.1.1.4.32.12	SECTION 1.81	1.81 Rejection of entry filing.

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