We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Accept
Home » Draft Guidance Outlines Good Importer Practices
Draft Guidance Outlines Good Importer Practices
January 16, 2009
To prevent potential contamination and counterfeiting, device importers regulated by the FDA need to know the foreign producers, consolidators, trading companies and distributors of their products and monitor them, a new draft guidance says.