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PRINTED: 11/20/2014 FORM APPROVEDDEPARTMENT OF HEALTH AND HUMAN SERVICES CENTERS FOR MEDICARE & MEDICAID SERVICES STATEMENT OF DEFICIENCIES AND PLAN OF CORRECTION(X1) PROVIDER/SUPPLIER/CIA IDENTIFICATION
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Individuals who have identified issues or concerns related to a regulated product or facility that fall under the jurisdiction of the FDA may need to fill out form 20d 483.
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20d 483 is a specific form or documentation used for filing certain regulatory information, typically related to compliance and reporting requirements.
Organizations or individuals who meet specific regulatory criteria must file 20d 483.
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The purpose of 20d 483 is to collect necessary data to ensure compliance with regulations and to monitor organizational or individual activities.
The information required on 20d 483 typically includes identifying details, compliance metrics, and any relevant activities that fall under the purview of the regulations.
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