Classification, Compliance Key to Avoiding Import Delays for Medical Devices
Monday, July 30, 2018 Sandler, Travis & Rosenberg Trade Report Properly classifying imports helps ensure a smooth transaction for any product but is especially important for items that are or might be considered medical devices regulated by the Food and Drug Administration, according to Shelly Garg, an attorney with Sandler, Travis & Rosenberg’s FDA practice. […]