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CBP AD and CV Messages as of July 31 - Aug. 2
August 3, 2018 |Customs

A listing of recent antidumping and countervailing duty messages from the Commerce Department posted to CBP's website July 31 to Aug. 2, along with the case number(s) and CBP message number, is provided below. The messages are available by searching for the listed CBP message number at CBP's ADD CVD Search page.

Comments on CBP's Drawback Rules Due Sept. 17
August 2, 2018 |Customs

CBP will accept comments on its proposed rules for drawback under the Trade Facilitation and Trade Enforcement Act until Sept. 17, the agency said in its notice published in the Aug. 2 Federal Register. The text of the noticed was released on July 27 (see 1807270024) and the drawback industry is looking closely at the proposal. "We are still in the many stages of review, we do know that there will be considerable comments that are made from all different trade groups," said Dave Corn, vice president of Comstock and Theakston, in an Aug. 2 email. "Among the big concerns is the change for excise taxes, transfers of merchandise, tracking new definitions throughout the package, etc. Now that we know comments are due September 17th, the big push will begin to complete a thorough review."

Topics:Drawback
CBP AD and CV Messages as of July 30-31
August 1, 2018 |Customs

A listing of recent antidumping and countervailing duty messages from the Commerce Department posted to CBP's website July 30-31, along with the case number(s) and CBP message number, is provided below. The messages are available by searching for the listed CBP message number at CBP's ADD CVD Search page.

CBP Finds Country of Origin for Needle Electrodes Is Either US or Japan, Based on Country of Manufacture
July 31, 2018 by Tim Warren|Customs

Needle electrodes from the U.S. or Japan that are sent to China for further processing remain products of the U.S. or Japan, CBP said in a ruling. Rhythmlink International, a manufacturer and distributor of medical devices, requested a final determination from CBP on the country of origin. Specifically, the company asked about "a Subdermal Needle Electrode," which is classified by the Food and Drug Administration as “a device which is placed subcutaneously to stimulate or to record electrical signals.”