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

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