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

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