MIL-PRF-27210J
4.5.1 Documentation of procedures. Written procedures that detail the sampling and testing
program and the analytical and measuring equipment calibration program shall be maintained.
4.5.2 Test reports. Test reports shall accompany each shipment and may be provided on the
contractor's internal form, a letter of transmittal, the product DD Form 250, or Wide Area Work Flow
(WAWF) electronic form. For Type I, the reports shall include the values obtained from the odor, fill
pressure, purity and moisture tests. For Type II, the reports shall include the values obtained from the
odor, purity, and moisture tests.
4.6 Filtration of Type II Oxygen. When required, Type II oxygen shall be passed through a filter
with a rating of at least 10-micrometer nominal (40-micrometer absolute) located in the fill line to the
shipping container.
5. PACKAGING
5.1 Packaging. For acquisition purposes, the packaging requirements shall be as specified in
the contract or order (see 6.2). When actual packaging of materiel is to be performed by DoD or in-house
contractor personnel, these personnel need to contact the responsible packaging activity to ascertain
packaging requirements. Packaging requirements are maintained by the Inventory Control Point's
packaging activities within the Military Service or Defense Agency, or within the military service's system
commands. Packaging data retrieval is available from the managing Military Department's or Defense
Agency's automated packaging files, CD-ROM products, or by contacting the responsible packaging
activity.
6. NOTES
(This section contains information of a general or explanatory nature that may be helpful, but is not
mandatory.)
6.1 Intended use. The oxygen covered by this specification is intended for use in military aircraft
breathing oxygen systems.
6.2 Acquisition requirements. Acquisition documents should specify the following:
a.
Title, number, and date of this specification.
b.
Type of oxygen required (see 1.2)
c.
First article inspection will be performed as specified in 4.2.
d.
The name and address of the laboratory to which the representative product specimen is
to be submitted (see 4.2, 6.4, and Table VI).
e.
When variation in points of inspection are granted (see 4.2.3.1).
f.
When variation in sampling method is granted (see 4.3.2).
g.
When a variation in analytical procedures is granted (see 4.5).
h.
Packaging requirements (see 5.1 and 6.3).
i.
Cylinder size, capacity and fill pressure (as determined by cylinder size and
capacity).
j.
When cleaning and repair schedule is required for leased or Government owned
containers.
k.
Method of shipment.
l.
A hydrostatic and/or ultrasonic testing, cleaning, and repair schedule for
cylinders that meets current DOT requirements.
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