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Site-Specific Health and Safety Plan (HASP) - Laschools.org

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SECTION 10<br />

CORRECTIVE ACTION<br />

The following procedures have been established to assure that conditions adverse to data<br />

quality are promptly investigated, evaluated, <strong>and</strong> corrected. Adverse conditions may<br />

include malfunctions, deficiencies, deviations, <strong>and</strong> errors.<br />

When a significant condition adverse to data quality is noted at the laboratory, the cause<br />

of the condition will be determined, <strong>and</strong> corrective action will be taken to prevent<br />

repetition. Condition identification, cause, reference documents, <strong>and</strong> corrective action<br />

planned will be documented <strong>and</strong> reported to the contractor QA officer by the laboratory<br />

QC coordinator. Following implementation of corrective action, the laboratory QC<br />

coordinator will report the actions taken <strong>and</strong> their results to the contractor project<br />

manager <strong>and</strong> QA officer. A record of the action taken <strong>and</strong> results will be attached to the<br />

data report package. If samples are reanalyzed, the assessment procedures will be<br />

repeated, <strong>and</strong> the control limits will be reevaluated to ascertain if corrective actions have<br />

been successful.<br />

Implementation of corrective action is verified by documented follow-up action. All<br />

project personnel have the responsibility, as part of the normal work duties, to identify,<br />

report, <strong>and</strong> solicit approval of corrective actions for conditions adverse to data quality.<br />

Corrective actions will be initiated in the following instances:<br />

• When predetermined acceptance criteria are not attained (objectives for precision,<br />

accuracy, <strong>and</strong> completeness);<br />

• When the prescribed procedure or any data compiled are faulty;<br />

• When equipment or instrumentation is determined to be faulty;<br />

• When the traceability of samples, st<strong>and</strong>ards, or analysis results is questionable;<br />

• When QA requirements have been violated;<br />

• When designated approvals have been circumvented;<br />

• As a result of systems or performance audits;<br />

• As a result of regular management assessments;<br />

• As a result of intralaboratory or interlaboratory comparison studies; <strong>and</strong><br />

• At any other instance of conditions significantly adverse to quality.<br />

10-1<br />

K:\Depts\Dept48\LAUSD\MSA WORK\QAPP\Draft Final QAPP to DTSC\QAPP for OU 1 RAP.DOC<br />

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