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Sunday, February 23, 2014, Napa Valley Marriott 3425 Solano Ave Napa, CA 94558 (707) 253-8600 Wednesday, October 15, 2014, Renaissance Palm Springs (preceding the CAP Conference) 888 E Tahiti Canyon
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How to fill out CAPA at NAPA:

01
Start by gathering all the necessary information and documentation for the CAPA form, such as the details of the nonconforming product or process, any identified root causes, and proposed corrective actions.
02
Clearly identify the nonconformance and specify its impact on quality, safety, or customer satisfaction.
03
Document all relevant information about the root cause of the nonconformance. This may include data analysis, investigations, or any other supporting evidence.
04
Develop appropriate corrective actions that address the identified root cause. These actions should be specific, measurable, achievable, relevant, and time-bound (SMART).
05
Assign responsibility for implementing the corrective actions to individuals or teams, ensuring accountability.
06
Define a timeline for implementing the corrective actions and specify any necessary resources or support required.
07
Follow up on the progress of the corrective actions and track them to completion. Regularly review the status and effectiveness of the actions.
08
Once the CAPA form is completed, obtain any necessary approvals or signatures from relevant personnel.
09
Keep a record of the CAPA form for future reference and continual improvement purposes.

Who needs CAPA at NAPA:

01
NAPA employees involved in quality control and assurance.
02
NAPA supervisors and managers responsible for addressing nonconformances.
03
NAPA executives who oversee quality management and continuous improvement initiatives.
04
Any other relevant stakeholders involved in maintaining and improving product and process quality at NAPA.
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CAPA stands for Corrective and Preventive Action, a process used to investigate and address quality issues within an organization.
Employees or individuals responsible for quality control or process improvement may be required to file CAPA at NAPA.
To fill out CAPA at NAPA, one must document the issue, root cause analysis, proposed corrective actions, and implementation plan.
The purpose of CAPA at NAPA is to improve processes, prevent quality issues, and ensure continuous improvement in product quality.
Information such as the issue description, root cause analysis, corrective actions, implementation plan, and verification of effectiveness must be reported on CAPA at NAPA.
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