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

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