Conformity Audits — Innovio FlexKapG

Conformity Audits give you objective evidence that a supplier's quality system, manufacturing process or specific product line genuinely meets the standard or regulation it is meant to comply with. We run process audits, system audits, and CE / regulatory readiness assessments — performed by experienced lead auditors — anywhere in your supply chain.

Capabilities

What's included.

Supplier Pre-Qualification

Capability and capacity audits before you place strategic POs with new suppliers.

ISO 9001 / 14001 / 45001

Full or partial system audits against the applicable management standard, with detailed findings register.

Process Audits

VDA 6.3, IATF 16949 process and product audits for automotive and industrial supply chains.

CE / Regulatory Readiness

Technical file review and gap analysis for CE marking under MDR, PED, MD, LVD and EMC directives.

How we work

Our process.

01

Audit Plan

Scope, criteria, audit team and schedule agreed with your team and the auditee.

02

Opening Meeting

Kick-off with the supplier — confirm scope, methodology and reporting format.

03

Audit Execution

Document review, process observation, interviews and evidence sampling on-site.

04

Closing & Report

Closing meeting, findings register (NC / OFI), and full audit report within 10 working days.

Deliverables

Audit plan and checklist
Findings register (NC, OFI, observations)
Full audit report with executive summary
Corrective action tracking through closure

Standards & Codes

ISO 19011 ISO 9001 / 14001 / 45001 IATF 16949 VDA 6.3 EU MDR / PED / MD / LVD

Industries served

Industrial Manufacturing Medical Devices Energy & Commodities Construction & Engineering

Ready to start your conformity audits project?

Talk to our engineering team to scope the work, agree the schedule, and receive a fixed quotation — usually within two working days.

Request a quote

Our Services

Conformity Audits.