MIL-PRF-19500P
APPENDIX E
E.3.7.2.1 Particle impact noise detector (PIND) test equipment failure or error. If it is determined through an
engineering evaluation and traceable through the manufacturer's quality system, that PIND rejects are the result of
equipment failure or human error, then all devices (passed and rejected) subsequent to the equipment failure or
human error, may be restarted. The devices shall be restarted at the run in which it was determined the equipment
failed or the human error occurred.
E.3.7.3 Standard mixer diodes and holders. The manufacturer of UHF and microwave mixer diodes shall establish
and maintain standard mixer diodes and standard mixer holders for use in qualification and quality conformance
testing of UHF and microwave mixer diodes. These standards shall be calibrated at least once in each successive
12-month period or prior to use if over 12 months, at a laboratory acceptable to the Government.
E.3.8 JANS electrical test data. Unless otherwise specified in the specification sheet, all electrical measurements
performed on devices after screen 8 of table E-IV shall be recorded and traceable to the serial number. This includes
all manufacturing imposed tests.
E.3.8.1 Summary of parts fallout. A summary of the JANS parts fallout during screening tests shall be prepared by
the manufacturer in accordance with the requirements of the qualifying activity
E.3.9 Preservation of lot identity. During all screening, inspection, and marking operations, each lot and sublot
shall be kept segregated, secure, and traceable.
E.4 VERIFICATION
E.4.1 Qualification inspection. Qualification inspection shall be performed at a facility approved by the qualifying
activity and shall be conducted in accordance with the procedures described herein for groups A, B, C, D, and E
inspection and by the qualifying activity. Qualification of a particular device type to a given quality level may be
extended by the qualifying activity to any other quality level provided all the groups A, B, C, D, and E requirements of
the other level have been met and provided that suitable approved screening facilities are available for the other tests
and stress levels. In addition, the requirements of appendix H shall be met. Small lot sampling shall not be used for
qualification inspection. Variables data is required for qualification. Manufacturers shall notify the qualifying activity
when a qualification lot is removed from consideration as a qualification lot. The manufacturer shall notify the
qualifying activity in writing within 35 days that the lot is being removed from consideration.
Group D is required for each inspection lot of RHA types as specified in the specification sheet. Qualification for
RHA shall be for a specific semiconductor die.
An alternate qualification procedure for RHA devices for levels M, L, and D only, are available for devices with
demonstrated RHA. These devices shall be submitted for qualification inspection and conformance inspection, if
process or design changes affecting RHA are made.
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