MIL-STD-1330 Precision Cleaning And Testing Of Shipboard Oxygen, Helium, Helium-Oxygen, Nitrogen, And Hydrogen SystemsThis standard provides the requirements for precision cleaning and testing of oxygen or oxygen-enriched systems and components; oxygen generating plants including nitrogen, hydrogen, and demineralized water support systems and components; and helium, helium-oxygen, and hydrogen life support systems and components. Each activity will implement the applicable requirements of this document through a locally prepared and approved procedure. Activities subject to additional quality assurance requirements such as NAVSEA SS800-AG-MAN-010/P-9290 or NAVSEA SS521-AA-MAN-010 will obtain procedure approval from the applicable certifying activity.

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MIL-STD-1330D(SH) APPENDIX D

w/ Change 1

DATA SHEET 3. Establishing Dish Acceptance Criteria.

EVAPORATING DISH:

Name and ID (e.g., badge): _Date:

Date evaporating dish was last calibrated:

Batch number for standard:

Solvent used for standard: (Shall be same as solvent used for cleaning the instrument.)

Baseline applies: Yes No ; if "yes" lot or batch #

Gain Settings: Sensor:

Control Unit:_

Clean Dish Acceptance Criteria

Reading and Average	SQM Readings
	Cleaning #1	Cleaning #2
Reading #1
Reading #2
Average for Reading #2 1/ (Clean Dish Acceptance Criteria)
NOTE: 1/ For reading #2, the difference between the readings shall be less than 100 counts.

Dish 5 ppm Acceptance Criteria

Reading/Dose and average	SQM readings
Reading/Dose and average	Trial 1	Trial 2	Trial 3
Cleaned Dish
Reading #1
Reading #2 2/
Dish 5 ppm Acceptance Criteria
Dose #3
Average Dose #3 3/ (Dish 5 ppm Acceptance Criteria)
NOTES: 2/ For all trials, for reading #2, the difference between the clean dish acceptance criteria and each result must be less than 100 counts. 3/ For dose #3, calculate the difference between the highest and lowest readings. If it meets the acceptance criteria in Table D-III or D-IV, as applicable, the data is acceptable. If it does not meet the acceptance criteria, perform additional trials until results are acceptable.