Rework Label Document For Free - Rework Document

Rework is an additional step in the production process to avoid unnecessary wastage. This procedure makes non-conforming or surplus materials removed from the line acceptable for reuse. All rework activities must result in safe product that meets minimum legal and quality standards.

Rework is defined as wholesome, salvageable product generated during a production run that is not acceptable as the approved finished end product on the end product schedule. Any raw product that does not go through the entire production process should not be considered rework.

The purpose of a Rework Procedure is to establish and maintain processes for rework for your organisation, including retesting and revaluation of the non-conforming product after rework is complete.

A rework procedure consists of the corrective actions when a product has failed to meet the specifications, and it's an integral part of any medical device production.

Rework is an additional step in the production process to avoid unnecessary wastage. This procedure makes non-conforming or surplus materials removed from the line acceptable for reuse. All rework activities must result in safe product that meets minimum legal and quality standards.

Rework is defined as wholesome, salvageable product generated during a production run that is not acceptable as the approved finished end product on the end product schedule. Any raw product that does not go through the entire production process should not be considered rework.

The purpose of a Rework Procedure is to establish and maintain processes for rework for your organisation, including retesting and revaluation of the non-conforming product after rework is complete.