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

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