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

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