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.

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New and Revised FDA Import Alerts for Sept. 28

October 1, 2012 by Brian Feito|FDA

On Sept. 28 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 Sept. 27

September 28, 2012 by Brian Feito|FDA

On Sept. 27 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 Sept. 26

September 28, 2012 by Brian Feito|FDA

The Food and Drug Administration issued its weekly Enforcement Report for Sept. 26 that lists the status of recalls and field corrections for food, drugs, biologics, and devices. The report covers both domestic and foreign firms.

New and Revised FDA Import Alerts for Sept. 26

September 27, 2012 by Brian Feito|FDA

On Sept. 26 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:

FDA Updates FAQ on FSMA Re-Registration and Suspension of Registration

September 27, 2012 by Brian Feito|FDA

The Food and Drug Administration updated its frequently asked questions on the Food Safety Modernization Act (FSMA) registration requirements, which require facilities that are required to register to re-register every two years, and provide for the suspension of facilities’ registration by the FDA. The re-registrations will begin in October -- December 2012. FDA has been able to suspend registration of facilities since July 3, 2011. New sections of the FAQ include:

New and Revised FDA Import Alerts for Sept. 25

September 26, 2012 by Brian Feito|FDA

On Sept. 25 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 Sept. 24

September 25, 2012 by Brian Feito|FDA

On Sept. 24 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 Sept. 17-23

September 25, 2012 by Brian Feito|FDA

During the week of Sept. 17-23, 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 Sept. 20

September 21, 2012 by Brian Feito|FDA

On Sept. 20 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 Sept. 19

September 21, 2012 by Brian Feito|FDA

The Food and Drug Administration issued its weekly Enforcement Report for Sept. 19 that lists the status of recalls and field corrections for food, drugs, biologics, and devices. The report covers both domestic and foreign firms.