Our facility has recently done a consolidation of finished good's profiles they are willing to produce in in order to focus on the products we do well from process capability standpoint and focused on highest volume customers or products in order to cut down unnecessary downtime and short runs.
This work has eliminated all products for two of my HACCP plans. So, I would like to archive those plans or designate them as "not active". They are FDA based plans, not sure if that really matters but what supporting documentation or assessment should be done in order to state they are not active plans and to prevent a GFSI auditor from reviewing them during our yearly audit?
The Management team is in agreement that there is not current plans to re-activate due to not being interested in products in those categories.
And I understand I cannot dispose of any of the previous documentation associated with the archived plans or products.
Just need a second opinion on proper next steps.