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

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