Title 21

PART 1 SUBPART D

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

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