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

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