Correction commonly refers to the action taken to eliminate a detected nonconformity or defect, without addressing its underlying cause.
Correction commonly refers to the immediate action taken to eliminate a detected nonconformity, defect, or other identified problem in a product, process, document, or record. It focuses on fixing what is wrong in the current instance so that the specific issue is resolved or contained.
In industrial and regulated manufacturing environments, corrections typically include:
Corrections can be physical (e.g., rework, repair, scrap) or administrative (e.g., issuing a corrected document, updating a log, reversing an incorrect transaction in MES or ERP).
A correction does not, by itself, remove the underlying cause of the nonconformity. It addresses the symptom that has already occurred, not the systemic reasons it occurred. Activities focused on root cause, recurrence prevention, or risk reduction are typically classified as corrective or preventive actions, not just corrections.
In quality management systems and shop-floor workflows, corrections are often:
Corrections may be part of a larger problem-solving or CAPA (Corrective and Preventive Action) process but are distinct from the investigation and systemic actions that follow.
In regulated environments, correcting records or documents (for example, changing an entry in an electronic batch record, router, or inspection report) generally requires controlled methods such as traceable amendments, reason codes, and audit trails. These are still considered corrections, but they must maintain data integrity and traceability.