Defects Fishbone Interview Check Meeting Process Why Standard Operating Procedure (SOP) Systemic Issue Fishbone Diagram Follow- up Pareto Chart CAPA Equipment Effect Gemba Walk Training Observation Symptom Data Collection Team Review Fault Tree Quality Plan Effect Analysis Document Prove it! Verification Preventive Action Problem Investigation Error Cause Drill Down Problem Statement Cause and Effect Solution Lessons Learned Test Timeline Ishikawa Failure Mode Deviation Environment System Failure Action Plan Risk Assessment Process Mapping Fix Human Documentation Rework Out-of- Spec 5 Whys Root Cause Validation Non- Conformance Report Human Error Standard Analysis Mistake Data Gap Corrective Action Causal Factors Downtime Brainstorming Containment Trigger Event Defects Fishbone Interview Check Meeting Process Why Standard Operating Procedure (SOP) Systemic Issue Fishbone Diagram Follow- up Pareto Chart CAPA Equipment Effect Gemba Walk Training Observation Symptom Data Collection Team Review Fault Tree Quality Plan Effect Analysis Document Prove it! Verification Preventive Action Problem Investigation Error Cause Drill Down Problem Statement Cause and Effect Solution Lessons Learned Test Timeline Ishikawa Failure Mode Deviation Environment System Failure Action Plan Risk Assessment Process Mapping Fix Human Documentation Rework Out-of- Spec 5 Whys Root Cause Validation Non- Conformance Report Human Error Standard Analysis Mistake Data Gap Corrective Action Causal Factors Downtime Brainstorming Containment Trigger Event
RCA - Call List(Print)
Defects
Fishbone
Interview
Check
Meeting
Process
Why
Standard Operating Procedure (SOP)
Systemic Issue
Fishbone Diagram
Follow-up
Pareto Chart
CAPA
Equipment
Effect
Gemba Walk
Training
Observation
Symptom
Data Collection
Team
Review
Fault Tree
Quality Plan
Effect Analysis
Document
Prove it!
Verification
Preventive Action
Problem
Investigation
Error
Cause
Drill Down
Problem Statement
Cause and Effect
Solution
Lessons Learned
Test
Timeline
Ishikawa
Failure Mode
Deviation
Environment
System Failure
Action Plan
Risk Assessment
Process Mapping
Fix
Human
Documentation
Rework
Out-of-Spec
5 Whys
Root Cause
Validation
Non-Conformance
Report
Human Error
Standard
Analysis
Mistake
Data
Gap
Corrective Action
Causal Factors
Downtime
Brainstorming
Containment
Trigger Event
