quality records

The quality records related to the product safety must be retained for at least fifteen years after the products are no longer produced.

The quality records exceeding retention period or without any reference values might be destroyed.

Is there a written procedure that defines how quality records are stored, protected and disposed of as well as a defined retention period?

Quality records shall be maintained to demonstrate conformance to specified requirements and the effective operation of the quality system.

Internal documents: quality manual, procedures, specifications, drawings, quality records, work instruction etc.

Pertinent quality records from the subcontractor shall be an element of this data.

The destroy of quality records must have destroy records. Implement the "Document & Data Control Procedures" .

Each functional department is responsible for filing of professional quality records within its respective business scope.

Quality Assurance Manager insures that the quality records maintenance procedure is enforced.

In the wake of the scandal, China has canceled inspection exemptions given to companies with proven quality records.

Completion of the daily quality records, statistic daily quality information.

Where agreed contractually are quality records available to the customer for evaluation for an agreed period?

Traceable quality records shall be complete, legible and normative. The retention period of records refers to relevant standard.

The Quality Dept. is responsible for keeping in file the quality records regarding corrective and preventive actions.

Is there a documented procedure defining the identification, storage, protection, retrieval, retention time and disposition quality records?

responsible for files management of inspection materials and quality records.

The Quality Department is responsible for the management of quality records.

i. Does the supplier maintain quality records that provide evidence of product conformity?

Work with the quality control teams located in the factory to maintain quality records properly.

Audit of all areas to include Document Control, Quality Records and Statistical Techniques, as appropriate.

And correlated data (including quality records) will be reserved for one year more after tooling is discarded.

Responsible to make quality records of the department according to relevant regulations.

A. Are quality records defined, identified, and retrievable ?

Protect quality records from unauthorized access.

Monitors retention and maintenance of quality records.

The implemented status and process control quality records for each plot.

the management of all quality records and decide the storage life and management department of all the quality records.

Make the correspondent quality records and summary statistics.

Remove, archive, and destroy old quality records.

Are quality records reviewed at the weekly QC meetings?

If client needs, our company can offer the quality manual and program files and 22 all quality records.

Review of the related quality records.

Do you store and retain quality records in a suitable environment to minimize deterioration or damage?

Keep archive of all quality records.

While performing the audit be alert for training, process control, doc. control and quality records issues

Documented system to define storage, protection and retention of quality records

Quality records to be filled out (eg. Check sheets)

familiar with the work required for ISO9000 certification quality records;

Quality documents and quality records

Finish inspection reports and other quality records in time;