QUALITY MANUAL (ISO/IEC 17025 : 2008)
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XXX/QM/16
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Control of nonconforming testing and or
calibration work
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Reference
ISO Clause
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4.9.1
The policy of laboratory is to
identify any of their testing or related activity not according to procedure or
not as per the agreed requirements of customer. The procedure SOP has been
documented and implemented to ensure that
a)
QAM is responsible in
consultation with TM.
b)
the TM is responsible and is
authorized to identify nonconforming work and actions initiated when
nonconforming work is identified;
c)
the significance and
severe-ness of nonconforming work is evaluated and corrective action is
promptly initiated;
d)
as based on information like
customer complaint, quality control, calibration of equipment, checking of
consumables used, logbook comments by testing personnel / supervisor,
verification of test / calibration results, internal / external audit reports
and management review.
e)
the customer is informed, the
test / calibration reports are called back if sent.
f)
TM has been made responsible
for the proposed corrective action that is to be undertaken and resumption of
work.
4.9.2
If felt that the
nonconformities may recur again, or that there is doubt about the compliance of
laboratory’s operations with its own policy and procedure, corrective action
procedure Quality Process SOP is initiated.
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