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This document outlines the findings from a state licensure survey conducted at Mason Valley Residence, including any deficiencies found and the facility's plan of correction. It documents compliance
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How to fill out STATEMENT OF DEFICIENCIES AND PLAN OF CORRECTION

01
Start by obtaining the STATEMENT OF DEFICIENCIES and PLAN OF CORRECTION form from the relevant regulatory body.
02
Carefully read the instructions provided with the form to understand the requirements.
03
Identify and document each deficiency as noted in the inspection report.
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For each deficiency, provide a detailed explanation of how it occurred, including any contributing factors.
05
Develop a plan of correction for each deficiency, outlining specific actions that will be taken to address the issue.
06
Assign responsibility for each action item to specific staff members or teams.
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Establish a timeline for the implementation of the corrective actions and include it in your plan.
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Review the filled-out form for accuracy and completeness, ensuring that all deficiencies and corrections are clearly stated.
09
Submit the completed form to the regulatory body by the specified deadline.
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Keep a copy of the submitted form for your records.

Who needs STATEMENT OF DEFICIENCIES AND PLAN OF CORRECTION?

01
Healthcare facilities that have been cited for deficiencies during inspections.
02
Organizations seeking to demonstrate compliance with regulatory standards.
03
Administrators and management teams responsible for quality assurance and improvement.
04
Regulatory bodies that require a formal response to identified deficiencies.
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There are three scope levels assigned to a deficiency: isolated, pattern, or widespread. The survey agency determines the scope and severity levels for each deficiency cited on a survey.
Element 1: How the corrective action will be accomplished for identified affected individuals. Element 2: How will other individuals with the potential to be affected or in similar situations be identified and protected. Element 3: What systemic changes will ensure that the deficient practice will not recur.
There are three scope levels assigned to a deficiency: isolated, pattern, or widespread. The survey agency determines the scope and severity levels for each deficiency cited on a survey.
An acceptable Plan of Correction will include both immediate corrective actions to correct the violation and long-term quality improvement actions, with each element including who is responsible, when it will be done, and what action has been or will be taken.
A facility is not required to submit a plan of correction when it has deficiencies that are isolated and have a potential for minimal harm, but no actual harm has occurred.
In all cases of immediate jeopardy, the provider agreement must be terminated by CMS or State Medicaid Agency no later than 23 calendar days from the last day of the survey if the immediate jeopardy is not removed.
To write a Statement of Deficiencies, three elements must be completed: • Gather enough strong evidence. Differentiate finding and deficient practice or noncompliance. Based on a regulation/requirement, recognize what the entity failed to do. Don't wait until near the end of the survey.

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The Statement of Deficiencies and Plan of Correction is a formal document that outlines any deficiencies identified during a facility's inspection or evaluation, along with a detailed plan to address and rectify those deficiencies.
Health care facilities that undergo inspections by regulatory bodies, such as nursing homes, assisted living facilities, and hospitals, are required to file a Statement of Deficiencies and Plan of Correction if deficiencies are found.
To fill out the Statement of Deficiencies and Plan of Correction, the facility must accurately document the deficiencies identified during the inspection, provide evidence of compliance, and outline specific steps and timelines for correction.
The purpose of the Statement of Deficiencies and Plan of Correction is to ensure that facilities take responsibility for identified issues, implement corrective measures, and maintain compliance with regulatory standards.
The information that must be reported includes a description of each deficiency, relevant citations from regulations, the facility's plan to resolve the issues, and a timeline for implementing the corrective actions.
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