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

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