The F.D.A. (Food and Drug Administration) is the agency within the U.S. Department of Health and Human Services that regulates access to the United States for both food and drugs. Registration with the F.D.A. is required of all companies that manufacture, process, package, or store food, beverages or drugs to be marketed in the United States.
The U.S. Federal Food, Drug and Cosmetic Act (FFDCA) defines labeling as all labels and other written, printed, or graphic matter on or accompanying any article or any of its containers or wrappers. The term accompanying is liberally construed to mean more than a physical association with the product. It extends to posters, labels, pamphlets, flyers, circulars, booklets, brochures, instructions, websites, etc. Labeling errors result in more than 22% of all arrests in the United States. LOCI helps companies modify food, medical device, cosmetic or drug labels to comply with F.D.A. regulations. Contact us, send us your product data sheet and we will review it.
We support you so that your exports to the USA are carried out successfully, complying with F.D.A. regulations in the food, beverage and cosmetics sectors.
If you need more details about our services, please send us a message.
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