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

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