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 Aug. 30 - Sept. 2

September 3, 2013 by Brian Feito|FDA

On Aug. 30 - Sept. 2 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 Aug. 29

August 30, 2013 by Brian Feito|FDA

On Aug. 29 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 Aug. 28

August 29, 2013 by Brian Feito|FDA

On Aug. 28 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 Aug. 28

August 29, 2013 by Brian Feito|FDA

The Food and Drug Administration issued its weekly Enforcement Report for Aug. 28 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 Aug. 27

August 28, 2013 by Brian Feito|FDA

On Aug. 27 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of:

FDA System Issues May Cause Entry Review Delays

August 28, 2013 by Claire Yan|FDA

Intermittent issues on Aug. 27 related with the Food and Drug Administration's application for manually reviewing entries may lead to delays beyond routine time frames in processing entries, CBP said. According to CBP, these issues are being investigated and district personnel have experienced higher caller volume as a result.

New and Revised FDA Import Alerts for Aug. 26

August 27, 2013 by Brian Feito|FDA

On Aug. 26 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 Aug. 20-26

August 27, 2013 by Brian Feito|FDA

During the week of Aug. 20-26, 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:

FDA Asks CBP for Careful Review, Notification of All Laser Pointer Imports

August 27, 2013 by Brian Feito|FDA

The Food and Drug Administration asked for notification of all imports of laser products so the agency can review admissibility, in an Aug. 12 letter to CBP. That includes informal and Section 321 low value entries, FDA said. The request for CBP notification is in response to mail and courier shipments of laser pointers that have been misdeclared as toys and flashlights to circumvent review, FDA said. The food, drug and device regulator needs to check if the laser pointers meet maximum energy output standards, it said.

New and Revised FDA Import Alerts for Aug. 23-25

August 26, 2013 by Brian Feito|FDA

On Aug. 23-25 the Food and Drug Administration posted new and revised versions of the following Import Alerts on the detention without physical examination of: