Hi, my company, a small facility, has recently successfully completed an SQF audit. I am new to the industry and do not have much experience with SQF and though we passed the audit, our auditor criticized many of our module 11 GMPs as being too broad and not specific enough to the facility. We are reluctant to make them specific as we are regularly changing production processes and even the structure of the facility as we grow. For example for things like storage plan, how specific are you? Do you include specific products and where they are stored, do you include how the allergens are separated or do you just say allergens are separated? Do you include where processing tools are kept or do you reference a procedure that already specifies it? Thank You
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