ISO 13485 & EU MDR / Preventive action
Is redesigning a faulty, non-conforming product a preventive action for future products or a corrective action for the faulty one?
Please select user.
ISO 13485 DOCUMENTATION TOOLKIT
Step-by-step implementation for smaller companies.
Find out more
Basically, it can be both. But, in my opinion, it is better to be preventive action.
HTML tags are not allowed