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PRINTED: 10/26/2021 FORM APPROVEDDivision of Health Service Regulation STATEMENT OF DEFICIENCIES AND PLAN OF CORRECTION(X1) PROVIDER/SUPPLIER/CIA IDENTIFICATION NUMBER’S T E P (SUMMIT TRAINING AND
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GAO-06-416 refers to a report by the Government Accountability Office (GAO) that assesses the quality of clinical laboratories and their compliance with regulations and standards.
Clinical laboratories that perform tests and diagnostics are required to file gao-06-416 clinical lab quality reports to ensure compliance with federal standards.
To fill out the gao-06-416 clinical lab quality report, laboratories must provide accurate data regarding their testing accuracy, compliance with regulations, and any quality control measures they employ.
The purpose of gao-06-416 clinical lab quality is to evaluate and enhance the quality of laboratory testing services, ensuring that they meet established standards and provide reliable results.
Laboratories must report information regarding test accuracy, quality control practices, staff qualifications, and any incidents of non-compliance or corrective actions taken.
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