- end products sold to customer
- ingredients
- packaging materials
I do not seem to be able to find clear requirements (not any) in FSSC (or other GFSI standards)
What are the legal requirements in key countries around the world (based on EFSA, FDA, etc).
Do you get customer requirements (if business to business) for your products for retention samples
If you have retention policy, how big should the retention sample (for each batch) be:
Enough to do all analysis once
Enough to do all analysis twice (in case of dispute give sample to independant lab)
(For documentation the situation is much clearer).
Thanks in advance for your help.







