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

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