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

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