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

U.S. FDA FCE-SID Korean Raspberry 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 Korean Raspberry products include:
  • Canned Korean Raspberry
  • Bottled Korean Raspberry
  • Jarred Korean Raspberry
  • Korean Raspberry in Pouch
  • Korean Raspberry in Tetra Pak
  • Korean Raspberry in Dressing
  • Marinated Korean Raspberry
  • Korean Raspberry in Water
  • Korean Raspberry in Oil
  • Korean Raspberry in Brine
  • Korean Raspberry in Sauce
  • Korean Raspberry in Syrup
  • Korean Raspberry in Spring Water
  • Korean Raspberry in Vinegar
Registrar Corp assists Korean Raspberry companies with:
  • FDA Korean Raspberry FCE Registration
  • FDA Korean Raspberry SID Process Filing
  • FDA Korean Raspberry FCE-SID Exceptions
  • FDA Korean Raspberry Label Requirements
  • FDA Korean Raspberry Import Information
  • FDA Korean Raspberry Detentions / Korean Raspberry Entry Refusals
  • General U.S. Food and Drug Administration Guidelines for:
    • Korean Raspberry Manufacturers
    • Korean Raspberry Suppliers
    • Korean Raspberry Processors
    • Korean Raspberry Exporters
    • Korean Raspberry Importers
In addition to Korean Raspberry Food Canning Establishment Registration (FCE) and Scheduled Process (SID) regulations, Korean Raspberry businesses are typically subject to U.S. FDA Food Facility Registration and U.S. Agent requirements (when applicable). For more information about Korean Raspberry 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













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