This QC Inspection Procedure complies with ISO 13485:2016, EU MDR 2017/745, and FDA QMSR 21 CFR 820. Delivered in editable Word format, it defines requirements for incoming, in‑process, and final inspection activities to ensure product conformity. Includes inspection criteria, documentation, and acceptance standards. Digital delivery within 24 business hours.
This procedure ensures consistent inspection and verification of materials, components, and finished products. It covers inspection planning, sampling, acceptance criteria, documentation, non‑conformance handling, and release authorization. Delivered in editable Word format for full customization. Consultancy support is available via email, Zoom, or on‑site visits. Full implementation or signed, approved procedures are available for an additional fee.