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

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