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

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