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PRINTED: 03/27/2017 FORM APPROVEDOffice of Health Care Quality STATEMENT OF DEFICIENCIES AND PLAN OF CORRECTION(X1) PROVIDER/SUPPLIER/CIA IDENTIFICATION NUMBER:(X2) MULTIPLE CONSTRUCTION A. BUILDING:
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01
To fill out a statement of deficiencies, follow these steps:
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Begin by entering the name and address of the facility that is being inspected.
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Clearly state the deficiency being observed, providing specific details and examples.
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Include any relevant regulations or requirements that are not being met.
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Offer suggestions for how the deficiency can be corrected or improved.
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Provide space for the responsible individual to acknowledge the deficiency and state the planned actions for correction.
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Sign and date the statement of deficiencies, and ensure that all necessary parties are notified.
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Keep a copy of the statement of deficiencies for your records and provide a copy to the facility being inspected.

Who needs statement of deficiencies x2?

01
Statement of deficiencies is needed by:
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- Regulatory agencies conducting inspections to assess compliance with regulations and standards.
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- Healthcare facilities and organizations to identify areas of improvement and ensure quality care.
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- Individuals or groups advocating for patient rights and safety.
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- Insurance companies or auditors conducting audits to evaluate the performance of facilities.
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- Legal entities involved in lawsuits or investigations related to healthcare facilities.
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A statement of deficiencies x2 is a formal document outlining specific areas within an organization that do not meet regulatory standards or requirements.
Organizations or entities that are subject to regulations and have identified deficiencies in their operations or compliance must file a statement of deficiencies x2.
To fill out a statement of deficiencies x2, you should provide detailed information about the deficiencies identified, corrective actions planned, and timelines for remediation.
The purpose of a statement of deficiencies x2 is to document compliance issues, facilitate corrective actions, and ensure accountability in meeting regulatory requirements.
Information such as the nature of the deficiencies, the context in which they occurred, actions taken to address them, and any relevant timelines must be reported.
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