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