📐 CQE Quest › Learn

5 Whys root-cause analysis

The 5 Whys is a question-driven root-cause analysis technique: you ask “Why did this happen?” repeatedly until you reach a systemic cause rather than a symptom. The name comes from a rule of thumb that five iterations typically reach the root cause, but the right number depends on the problem—it may be three or it may be seven.

The technique was developed by Sakichi Toyoda and is central to the Toyota Production System. It is a core tool in lean, Six Sigma, and ISO 9001 corrective-action processes.

How to run a 5 Whys

  1. Write a precise, factual problem statement (avoid vague language).
  2. Ask “Why did this happen?” and write the immediate cause.
  3. Ask “Why did that happen?” about the cause you just wrote.
  4. Repeat until you reach a root cause you can act on—a broken or missing system, process, or standard.
  5. Verify the chain by reading it backwards: “[root cause] leads to [cause 4], which leads to [cause 3]...”

Worked example

Problem: A batch of 2,000 tablets shipped to the customer with no certificate of analysis.

Corrective action: Add a rule to the batch release SOP requiring QA routing at least 24 hours before planned ship. Add a system check that flags batches scheduled to ship without a completed QA review.

Common exam traps

Test yourself in 2 minutes

Try 5 free CQE practice questions on this exact topic. Every wrong answer comes with an explanation. No account needed.

Take the free CQE quiz

More: 5 Whys · 8D problem solving · AOQ & AOQL · APQP & PPAP · AQL sampling plans · Attribute agreement & kappa · Attribute control charts · Availability & maintainability · Benchmarking types · Binomial vs Poisson · Blocking & randomization · Calibration & traceability · Capability: non-normal · Chi-square test · Confidence intervals · Control chart selection · Control plan · CA effectiveness · Cost of quality · Cp vs Cpk vs Cpm · Cpk vs Ppk · CQE exam day tips · CQE study plan · CQE vs CQA vs CSSBB · Is the CQE worth it? · CUSUM & EWMA · Design reviews · Design V&V · Destructive testing · DFMEA vs PFMEA · Document control · Fault tree analysis · First article inspection · Fishbone diagram · FMEA: RPN vs AP · Full vs fractional factorial · Gage R&R · GD&T basics · Hazard vs risk vs harm · Hypothesis test selection · I-MR chart · Interaction plots · ISO 14971 · ISO 9001 clauses · Kaizen event planning · Kano model · Lean wastes (TIMWOODS) · Linear regression · Management review · MRB dispositions · MSA: bias, linearity & stability · NCR, CAPA & PA · Nonparametric tests · Normal distribution & z-table · One-way ANOVA · p-value explained · Pareto chart · PDCA vs DMAIC · Poka-yoke · QFD / House of Quality · Quality audits · Quality mgmt principles · Quality manual vs procedures · Quality plan vs control plan · Redundancy: parallel & standby · Reliability allocation · Bathtub curve & MTBF · Response surface methods · Risk-based thinking · Risk matrix vs FMEA · 7 mgmt & planning tools · Short-run SPC · Six Sigma certifications · Sigma level & DPMO · Six Sigma DMAIC · Supplier quality scorecards · Switching rules (sampling) · Taguchi loss function · Theory of constraints · Tolerance stackup · Traceability & lot control · Type I vs II error · Value stream mapping · Variables vs attributes · Weibull analysis · Western Electric rules · X-bar R vs X-bar S · CQE calculators · Study planner · Section quiz

CQE Quest by Bizarre Act. Original study material; not affiliated with ASQ. CQE is a certification of ASQ. Terms · Privacy