Shopping Cart: 0 items
Your cart is empty.
MENU

FDA - US Domestic Food Facility Registration

  • FDA 510(K) APPLICATIONS/ SUBMISSIONS
    FDA 510(K) APPLICATIONS/ SUBMISSIONS
    FDA APPLICATIONS/ SUBMISSIONS In 1938 congress passed a set of laws giving authority to the U.S. Food and Drug Administration (FDA) to oversee the safety of food, drugs, and cosmetics. Section 510(k) requires Medical Device manufacturers to register and notify FDA, at least 90 days in advance, of their intent to market a medical device in the USA. This is called the Premarket Notification (PMA).... FDA APPLICATIONS/ SUBMISSIONS In 1938 congress passed a set of laws giving auth...
  • US Domestic Food Facility Registration and US Agent Services
    US Domestic Food Facility Registration and US Agent Services
    US domestic food facility registration ?Annual US agent communication service ?Free electronic certificate Free modification US domestic food facility registration ?Annual US agent communication service ?...