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

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