21 CFR Part 1005 - IMPORTATION OF ELECTRONIC PRODUCTS
- SUBPART A — General Provisions (§§ 1005.1 - 1005.3)
- SUBPART B — Inspection and Testing (§§ 1005.10 - 1005.11)
- SUBPART C — Bonding and Compliance Procedures (§§ 1005.20 - 1005.25)
Title 21 published on 2012-04-01
The following are only the Rules published in the Federal Register after the published date of Title 21.
For a complete list of all Rules, Proposed Rules, and Notices view the Rulemaking tab.
This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.
This list is taken from the Parallel Table of Authorities and Rules provided by GPO [Government Printing Office].
It is not guaranteed to be accurate or up-to-date, though we do refresh the database weekly. More limitations on accuracy are described at the GPO site.
§ 360ii - Program of control
§ 360mm - Imports
Title 21 published on 2012-04-01
The following are ALL rules, proposed rules, and notices (chronologically) published in the Federal Register relating to 21 CFR 1005 after this date.
GPO FDSys XML | Text type regulations.gov FR Doc. 2013-06864 RIN Docket No. FDA-2007-N-0091 (formerly 2007N-0104) DEPARTMENT OF HEALTH AND HUMAN SERVICES, Food and Drug Administration Final rule; technical amendment. This rule is effective March 26, 2013 21 CFR Part 1005 The Food and Drug Administration (FDA) is amending a final rule that appeared in the Federal Register of April 9, 2007 (72 FR 17397 at 17401) to reflect changes to the Center for Devices and Radiological Health's address. This action is editorial in nature and is intended to improve the accuracy of the Agency's regulations.