EAPA Litigation

Under the Enforce and Protect Act, CBP investigates whether a company is evading particular antidumping and countervailing duty orders. Litigation on determinations made under the relatively new statute have centered on due process protections for respondents, CBP's evidentiary basis for its decisions and the interplay of decisions made on the scope of the applicable AD/CVD orders from both CBP and the Commerce Department. The Court of Appeals for the Federal Circuit issued a key decision for all EAPA cases in Royal Brush Manufacturing v. United States, when it found CBP to have violated a respondent's due process protections by failing to provide it with access to the business proprietary information used in the proceeding.

Date Range:

Author:

Topic:

Refine Category Search

Clear Terms

Search Primer

Multi-word term: Place inside quotes to ensure an exact match together (e.g. "China import").

Term list: Separate terms with spaces, not commas or semicolons to find either word (e.g. AD/CVD antidumping).

Acronyms: Use all capital letters (e.g., ACE).

Required term: If a term must be included in any resulting articles, prefix it with a plus sign (e.g., CBP +releases).

Excluded term: If a term should be excluded from any articles being found, prefix it with a minus sign (e.g., -ruling).

Singular form: Use the singular form when doing multi-word terms (e.g. "russian export control" instead of "russian export controls").

Shortest word form: When you have different word forms in a quoted term, include the shortest version if it is the last part of the expression (e.g., "entity list" instead of "entity listing" or "entity listed").

New and Revised FDA Import Alerts for July 14

July 15, 2014 by Brian Feito|FDA

On July 14 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:

Other Modified FDA Import Alerts for the Week of July 7-13

July 15, 2014 by Brian Feito|FDA

During the week of July 7-13, the Food and Drug Administration modified the following existing Import Alerts (not otherwise listed on the FDA's new and revised import alerts page) on the detention without physical examination and/or surveillance of:

New and Revised FDA Import Alerts for June 10-11

July 14, 2014 by Brian Feito|FDA

On July 10-11 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:

FDA Enforcement Report on Recalls & Field Corrections for July 9

July 11, 2014 by Brian Feito|FDA

The Food and Drug Administration issued its weekly Enforcement Report for July 9 that lists the status of recalls and field corrections for food, drugs, biologics, and devices. The report covers both domestic and foreign firms.

FDA Issues July Interstate Certified Shellfish Shippers List

July 10, 2014 by Brian Feito|FDA

The Food and Drug Administration issued the Interstate Certified Shellfish Shippers List (ICSSL) for July . The ICSSL is published monthly for the information and use by food control officers, the seafood industry and other interested persons. The shippers listed have been certified by regulatory authorities in the U.S., Canada, Chile, South Korea, Mexico and New Zealand under the uniform sanitation requirements of the National Shellfish Program.

New and Revised FDA Import Alerts for July 8

July 9, 2014 by Brian Feito|FDA

On July 8 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:

FDA to Begin Requiring Monthly Tobacco Importer Reports in October

July 9, 2014 by Brian Feito|FDA

The Food and Drug Administration is amending its regulations to require monthly reports by tobacco importers and domestic manufacturers. The monthly reports are currently required by the U.S. Department of Agriculture under the Fair and Equitable Tobacco Reform Act’s Tobacco Transition Payment Program, but FDA is taking over because the USDA reporting program is ending in September and FDA still needs the information in order to calculate tobacco user fees. The information required in the monthly reports to FDA will be “essentially the same” as the elements currently required by USDA, as will the method by which FDA calculates user fees, it said. The first monthly reports will be due to FDA by Oct. 20.

New and Revised FDA Import Alerts for July 7

July 8, 2014 by Brian Feito|FDA

On July 7 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:

Other Modified FDA Import Alerts for the Week of June 30 - July 6

July 8, 2014 by Brian Feito|FDA

During the week of June 30 - July 6, the Food and Drug Administration modified the following existing Import Alerts (not otherwise listed on the FDA's new and revised import alerts page) on the detention without physical examination and/or surveillance of:

New and Revised FDA Import Alerts for July 3

July 7, 2014 by Brian Feito|FDA

On July 3 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of: