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