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HomeFood and BeveragesFCE (Food Canning Establishment) and SID (Process Filings)U.S. FDA FCE-SID Examples › Antipasto-Hors d'ouvere Regulations

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