FDA
The American Medical Device Market
To export medical devices to the United States, FDA approval is required. Certification procedures vary depending on the product classification.
To export medical devices to the United States, FDA approval is required. Certification procedures vary depending on the product classification.
U.S. tariffs under Section 301 of the Trade Act of 1974
Exemptions from the U.S. Tariff under Section 301
Business domiciliation in the United States and headquarters address for American subsidiaries
ExportUSA is the perfect choice if you are seeking a U.S.-based service provider that can assist with the incorporation, ongoing management, and tax compliance of a U.S. company that will be wholly owned by a foreign parent company.
Request for Refund of American Tariffs
Refund of US customs duties for defective products re-exported to Italy
FDA registration, appointment of an FDA Agent, label review, creation of nutrition facts: steps to follow to comply with the FDA
Difference between LLC and LP - Limited Partnership