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Food Facility Registration for U.S. companies that are engaged in producing, packing, or holding food.
A domestic facility that is engaged in manufacturing/processing, packing, or holding of food for human or animal consumption in the United States, must register with FDA, whether or not the food from the facility
enters interstate commerce (21 CFR 1.225(b)).
This is a bi-annual fee.
Commercial processors who manufacture, process, or pack acidified foods (AF) and/or thermally processed low-acid foods packaged in hermetically sealed containers (historically referred to as “low-acid canned foods” or “LACF”) must register their facility as FCE (Food Canning Establishment) 21 CFR 108.25(c)(1) (for AF) or 21 CFR 108.35(c)(1) (for LACF). They also need to file the processes 21 CFR 108.25(c)(2) (for processors of AF) or 21 CFR 108.35(c)(2) (for processors of LACF), and submit to FDA iths Schedule Process filings for for all of its commercially sterile, acidified and low-acid canned foods to obtain a Scheduled Process Identification (SID) Number from FDA for each specific canned food and aseptic or acidified food process.
TABS will assist you with the SID filings and registrations.
Food Facility Registration for U.S. companies that are engaged in producing, packing, or holding food.
A domestic facility that is engaged in manufacturing/processing, packing, or holding of food for human or animal consumption in the United States, must register with FDA, whether or not the food from the facility
enters interstate commerce (21 CFR 1.225(b)).
This is a bi-annual fee.
Food Facility Registration for U.S. companies that are engaged in producing, packing, or holding food.
A domestic facility that is engaged in manufacturing/processing, packing, or holding of food for human or animal consumption in the United States, must register with FDA, whether or not the food from the facility
enters interstate commerce (21 CFR 1.225(b)).
This is a bi-annual fee.
If during the year there are any changes in the existing drug listing, the drug listing should be updated immediately.
Any update outside the 3-month period will require submission for each NDC to certify the product.
