Our medical device company will be moving (to a location about 10 minutes away) within the next couple of months. With regard to FDA and ISO 13485:2016, do we need to relabel all of the products that are labelled with the old address, or do we just label the new products with the updated label going forward? The current label already has a valid e-mail address and the company website listed, so customers and distributors will be able to contact us, and the US Postal Service will be forwarding any mail to the new address. We have thousands of products on the shelf and relabeling each of them would be a daunting task. Any advice would be appreciated.