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HomeFood and BeveragesFCE (Food Canning Establishment) and SID (Process Filings)U.S. FDA FCE-SID Examples › Green Bean Drink Regulations

U.S. FDA FCE-SID Green Bean Drink Requirements



Food canning establishments in the United States and foreign establishments that process and export foods to the United States are subject to regulations that require registration of the establishments (FCE) and filing of scheduled processes (SIDs). The FCE registration and SID regulations for thermally processed low-acid and acidified foods packaged in hermetically sealed containers are found in Title 21 CFR 113 and 114. Typical hermetically sealed Green Bean Drink products include:
  • Canned Green Bean Drink
  • Bottled Green Bean Drink
  • Jarred Green Bean Drink
  • Green Bean Drink in Pouch
  • Green Bean Drink in Tetra Pak
  • Green Bean Drink in Dressing
  • Marinated Green Bean Drink
  • Green Bean Drink in Water
  • Green Bean Drink in Oil
  • Green Bean Drink in Brine
  • Green Bean Drink in Sauce
  • Green Bean Drink in Syrup
  • Green Bean Drink in Spring Water
  • Green Bean Drink in Vinegar
Registrar Corp assists Green Bean Drink companies with:
  • FDA Green Bean Drink FCE Registration
  • FDA Green Bean Drink SID Process Filing
  • FDA Green Bean Drink FCE-SID Exceptions
  • FDA Green Bean Drink Label Requirements
  • FDA Green Bean Drink Import Information
  • FDA Green Bean Drink Detentions / Green Bean Drink Entry Refusals
  • General U.S. Food and Drug Administration Guidelines for:
    • Green Bean Drink Manufacturers
    • Green Bean Drink Suppliers
    • Green Bean Drink Processors
    • Green Bean Drink Exporters
    • Green Bean Drink Importers
In addition to Green Bean Drink Food Canning Establishment Registration (FCE) and Scheduled Process (SID) regulations, Green Bean Drink businesses are typically subject to U.S. FDA Food Facility Registration and U.S. Agent requirements (when applicable). For more information about Green Bean Drink requirements, simply choose one of the options below:




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U.S. FDA Regulations:

U.S. FDA FCE/SID: 21 C.F.R. sections 108, 109, 113, 114













Registrar Corp assists businesses with U.S. FDA compliance. Certificates of Registration issued by Registrar Corp provide confirmation to industry that you are fulfilling U.S. FDA registration requirements. U.S. FDA does not issue or recognize Certificates of Registration. Registrar Corp is not affiliated with the U.S. Food and Drug Administration.

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