I have read through the threads regarding the sauce-making business and still have a bit of confusion. I am currently a hobby sauce maker in the process of becoming official. I am going the route of renting a commercial kitchen by the hour and selling locally. After getting local Food Manager Certificate and starting LLC and generally checking off the boxes, I had someone ask me about the stringent FDA regulations for shelf stable products. I assumed they were talking about low acidity foods but found that FDA regulations (114 CFR) about acidified foods were ponderous.
My question is to commercial hot sauce makers (on any scale, but preferably small to mirror my own ambitions). Do you have to keep samples from every batch for future problems and testing, does the FDA require any particular licensing and/or fees in addition to the local authorities? Other than keeping detailed pH testing data and production dates, do these regulations require anything? Do you have new batch numbers on the label for each production run?
Sorry for the preponderance of words, but that is how the inside of my head looks after looking through the Code of Federal Regulations as expressed by the FDA.
Any clarification or humor appreciated.
Thanks.
My question is to commercial hot sauce makers (on any scale, but preferably small to mirror my own ambitions). Do you have to keep samples from every batch for future problems and testing, does the FDA require any particular licensing and/or fees in addition to the local authorities? Other than keeping detailed pH testing data and production dates, do these regulations require anything? Do you have new batch numbers on the label for each production run?
Sorry for the preponderance of words, but that is how the inside of my head looks after looking through the Code of Federal Regulations as expressed by the FDA.
Any clarification or humor appreciated.
Thanks.