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

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