1-Minute Summary Pick a lab with an ISO 17025 scope that matches your matrix/analyte; use LAAF when your analyte is active on FDA’s Dashboard. Require validated, matrix-appropriate methods, with LOQ/LOD below the limit and full QC so results are defensible. ...
Reviewed and Approved by Tim Lombardo, Sr. Dir., Food Consulting Services, EAS Consulting Group; and Annie Hughes, Director, General Manager FDA Detention, Certified Group 1-Minute Summary FDA Red List removal requires proving the issue that caused detention has...
Reviewed and Approved by Tim Lombardo, Sr. Dir. of Food Consulting Services, EAS Consulting Group; Annie Hughes, Director, General Manager FDA Detention, Certified Laboratories FDA detentions are on the rise. In 2025 alone, the Agency reviewed nearly 50 million...
One of the most challenging aspects of doing business in the U.S. is navigating the many and varied regulatory requirements of U.S. agencies. When working with food imports overseen by the Food and Drug Administration (FDA) and United States Department of Agriculture...
When importing FDA-regulated food products into the USA, an FDA Notice of Action can be a challenging hurdle to overcome. It indicates potential non-compliance and may result in FDA detention, delaying or denying entry of your goods. The U.S. FDA oversees the safety...
