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 May 14

May 15, 2020 |FDA

On May 14 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 May 13

May 15, 2020 |FDA

The Food and Drug Administration issued its weekly Enforcement Report for May 13 that lists the status of recalls and field corrections for food, cosmetics, tobacco products, drugs, biologics and devices. The report covers both domestic and foreign firms.

FDA Adds Two More Importers to Import Alert 99-41 for FSVP Violations

May 15, 2020 |FDA

The Food and Drug Administration has added two more importers to Import Alert 99-41 for importers that aren’t in compliance with Foreign Supplier Verification Program requirements. Dinamix Distribution was added May 13, after being sent a warning letter in December that said the company did not set up FSVP programs for its imported mayonnaise and two types of drinks. One day later, FDA added El Molino Bakery Supplies, also after a December warning letter that said it hadn’t set up FSVPs. Both warning letters had been released by FDA in January (see 2001240037). Dinamix and El Molino are the second and third importers added to Import Alert 99-41, respectively. Brodt Zenatti remains on import alert, after having been added in October (see 1910210063).

New and Revised FDA Import Alerts for May 8-13

May 14, 2020 |FDA

On May 8-13 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:

New and Revised FDA Import Alerts for May 6

May 7, 2020 |FDA

On May 6 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 May 6

May 7, 2020 |FDA

The Food and Drug Administration issued its weekly Enforcement Report for May 6 that lists the status of recalls and field corrections for food, cosmetics, tobacco products, drugs, biologics and devices. The report covers both domestic and foreign firms.

FDA Withdraws Approvals for Some Chinese Mask Makers

May 7, 2020 |FDA

The Food and Drug Administration took away approvals for more than 60 mask makers in China to export masks similar to N95 into the U.S., The Wall Street Journal said in a May 7 report. The withdrawals are due to quality issues found by federal regulators with the imported products, the report said. The FDA last month said it would allow for imports of foreign respirators, including the KN95 from China (see 2004060052).

New and Revised FDA Import Alerts for May 4

May 5, 2020 |FDA

On May 4 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:

New and Revised FDA Import Alerts for May 1

May 4, 2020 |FDA

On May 1 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:

New and Revised FDA Import Alerts for April 30

May 1, 2020 |FDA

On April 30 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of: