A Supplier Corrective Action Report is a formal record used when a supplier sends defective, wrong, or late materials that cause a problem — either internally or for a customer. It documents what went wrong, why it happened, and what the supplier (and Canwil) need to do to fix it. SCAR records form the ISO 9001 audit trail for quality incidents.
If defective material needs to be returned to the vendor, flag RMA Required when opening the SCAR. Track the RMA status through: Pending → Issued → Received → Credited. This keeps the return and credit memo tied to the original quality incident.
If the defect reached a customer — delayed their order, required a replacement, or generated a complaint — document it in the Customer Impact field. This links the customer claim to the vendor root cause, which is exactly what ISO 9001 clause 8.7 requires for traceability of nonconforming outputs.
The Intelligence Scanner will eventually suggest opening a SCAR when it detects a pattern — for example, the same vendor flagged in 3 customer complaints within 60 days. You'll see a prompt in the scanner dashboard. You still review and confirm before it's opened.