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Page Title: CHAPTER 4. QUALITY ASSURANCE (QA)
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TB 750-25
4-1. General. The QA program, in accordance with AR 750-43 and the USATA SOP
702-1, assures that a standard system for TMDE support activities providing C&RS is
maintained. The QA program assures calibration and repair program compliance,
measurement accuracy, technical proficiency, product quality, and customer satisfaction.
4-2. QA Inspections
a. All activities inspected will be rated as to pass or fail. At the discretion of the
inspection team chief, a failing rating can result in the suspension of calibration support
by the inspected activity.
The functional areas subject to inspection include
management, operations, RADIAC, safety, facilities, and external support. One of the
following ratings are assigned to each functional area reviewed:
(1) No Deficiencies: Functional areas meet prescribed requirements.
(2) Deficiencies-None Failing: Performance did not meet prescribed requirements, but
were corrected and verified by the inspection team.
(3) Deficiencies-Failing, Resolution Required: Assigned when one or more
findings exist which are not or cannot be corrected for verification by the inspection
team.
(4) Deficiencies- Failing; Correction Verified:  Assigned when one or more
findings exist, but were corrected and the corrected findings were verified by the
inspection team.
(5) Deficiencies-Failing; Reinspection Required: May be assigned when one or
more critical findings exist, or the severity of a finding indicates the need for
reinspection. Furthermore, a rating of "deficiencies: failing; reinspection required" may
be the basis for recommending that instrument support operations be discontinued until
the deficiency/deficiencies are corrected. A rating of "deficiencies-failing; reinspection
required" will be assigned by the QA inspection team chief. Unresolved issues are
presented to the Director, USATA, for resolution.
b. Critical Finding. Critical findings that can cause an organization to fail overall,
or in a functional area, are:
(1) Failure of an end item to meet specifications.
(2) Loss of measurement traceability.
(3) Significant safety or health hazard.

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