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

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