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

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