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

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













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