Airworthiness Directives; AVOX System Inc. (Formerly Scott Aviation) Oxygen Cylinder and Valve Assemblies and Oxygen Valve Assemblies, 10958-10964 [2022-04146]
Download as PDF
10958
Federal Register / Vol. 87, No. 39 / Monday, February 28, 2022 / Rules and Regulations
(i) European Union Aviation Safety Agency
(EASA) AD 2021–0181, dated July 30, 2021.
(ii) [Reserved]
(3) For EASA AD 2021–0181, contact
EASA, Konrad-Adenauer-Ufer 3, 50668
Cologne, Germany; telephone +49 221 8999
000; email ADs@easa.europa.eu; internet
www.easa.europa.eu. You may find this
EASA AD on the EASA website at https://
ad.easa.europa.eu.
(4) You may view this material at the FAA,
Airworthiness Products Section, Operational
Safety Branch, 2200 South 216th St., Des
Moines, WA. For information on the
availability of this material at the FAA, call
206–231–3195.
(5) You may view this material that is
incorporated by reference at the National
Archives and Records Administration
(NARA). For information on the availability
of this material at NARA, email
fr.inspection@nara.gov, or go to: https://
www.archives.gov/federal-register/cfr/ibrlocations.html.
Issued on February 17, 2022.
Lance T. Gant,
Director, Compliance & Airworthiness
Division, Aircraft Certification Service.
[FR Doc. 2022–04147 Filed 2–25–22; 8:45 am]
BILLING CODE 4910–13–P
DEPARTMENT OF TRANSPORTATION
Federal Aviation Administration
14 CFR Part 39
[Docket No. FAA–2020–0345; Product
Identifier 2019–NM–154–AD; Amendment
39–21951; AD 2022–04–09]
RIN 2120–AA64
Airworthiness Directives; AVOX
System Inc. (Formerly Scott Aviation)
Oxygen Cylinder and Valve
Assemblies and Oxygen Valve
Assemblies
Federal Aviation
Administration (FAA), DOT.
ACTION: Final rule.
AGENCY:
The FAA is adopting a new
airworthiness directive (AD) for certain
AVOX System Inc. (formerly Scott
Aviation) oxygen cylinder and valve
assemblies, and oxygen valve
assemblies, installed on but not limited
to various transport airplanes. This AD
was prompted by reports of cylinder
and valve assemblies having oxygen
leakage from the valve assembly vent
hole, caused by the absence of a guide
that maintains appropriate spacing
between certain parts. This AD requires
an inspection of the oxygen valve
assemblies, and oxygen cylinder and
valve assemblies, to determine the serial
number of the valve, cylinder, and
entire assembly. For assemblies and
parts with certain serial numbers, this
khammond on DSKJM1Z7X2PROD with RULES
SUMMARY:
VerDate Sep<11>2014
16:12 Feb 25, 2022
Jkt 256001
AD requires a detailed inspection for
correct spacing of the gap between the
bottom of the packing retainer and top
of the valve body on the assemblies, and
replacement of assemblies having
unacceptable gaps. The FAA is issuing
this AD to address the unsafe condition
on these products.
DATES: This AD is effective April 4,
2022.
The Director of the Federal Register
approved the incorporation by reference
of certain publications listed in this AD
as of April 4, 2022.
ADDRESSES: For service information
identified in this final rule, contact
AVOX Systems Inc., 225 Erie Street,
Lancaster, NY 14086; telephone 716–
683–5100; internet https://
www.safranaerosystems.com. You may
view this service information at the
FAA, Airworthiness Products Section,
Operational Safety Branch, 2200 South
216th St., Des Moines, WA. For
information on the availability of this
material at the FAA, call 206–231–3195.
It is also available at https://
www.regulations.gov by searching for
and locating Docket No. FAA–2020–
0345.
reports of cylinder and valve assemblies
having oxygen leakage from the valve
assembly vent hole, caused by the
absence of a guide that maintains
appropriate spacing between certain
parts. In the NPRM, the FAA proposed
to require an inspection of the oxygen
valve assemblies, and oxygen cylinder
and valve assemblies, to determine the
serial number of the valve, cylinder, and
entire assembly. For assemblies and
parts with certain serial numbers, the
NPRM proposed to require a detailed
inspection for correct spacing of the gap
between the bottom of the packing
retainer and top of the valve body on the
assemblies, and replacement of
assemblies having unacceptable gaps
(removing affected assemblies and
installing serviceable assemblies). The
NPRM also proposed to require
reporting and returning of affected parts
to the manufacturer. The FAA is issuing
this AD to address oxygen leakage from
the cylinder, which could result in
decreased or insufficient oxygen supply
during a depressurization event; and
heating or flow friction, which could
cause an ignition event in the valve
assembly.
Examining the AD Docket
You may examine the AD docket at
https://www.regulations.gov by
searching for and locating Docket No.
FAA–2020–0345; or in person at Docket
Operations between 9 a.m. and 5 p.m.,
Monday through Friday, except Federal
holidays. The AD docket contains this
final rule, any comments received, and
other information. The address for
Docket Operations is U.S. Department of
Transportation, Docket Operations, M–
30, West Building Ground Floor, Room
W12–140, 1200 New Jersey Avenue SE,
Washington, DC 20590.
FOR FURTHER INFORMATION CONTACT:
Elizabeth Dowling, Aerospace Engineer,
Mechanical Systems and Administrative
Services Section, FAA, New York ACO
Branch, 1600 Stewart Avenue, Suite
410, Westbury, NY 11590; telephone
516–228–7300; email 9-avs-nyaco-cos@
faa.gov.
SUPPLEMENTARY INFORMATION:
Discussion of Final Airworthiness
Directive
Background
The FAA issued a notice of proposed
rulemaking (NPRM) to amend 14 CFR
part 39 by adding an AD that would
apply to certain AVOX System Inc.
(formerly Scott Aviation) oxygen
cylinder and valve assemblies, and
oxygen valve assemblies, installed on
but not limited to various transport
airplanes. The NPRM published in the
Federal Register on May 1, 2020 (85 FR
25353). The NPRM was prompted by
PO 00000
Frm 00034
Fmt 4700
Sfmt 4700
Comments
The FAA received comments from
one commenter, Air Line Pilots
Association, International (ALPA), who
supported the NPRM without change.
The FAA received additional
comments from five commenters,
including American Airlines (AAL),
Delta Air Lines (DAL), FedEx Express
(FedEx), United Airlines (UAL), and an
individual. The following presents the
comments received on the NPRM and
the FAA’s response to each comment.
Request To Revise Applicability
AAL and UAL suggested revising the
applicability statement to include more
aircraft manufacturers and models. AAL
suggested adding all airplane models
that affected assemblies could be
installed on, in particular, Boeing Model
737–NG (Next Generation models are
737–600, –700, –700C, –800, –900, and
–900ER series), 737–MAX, 777–200, and
777–300 series airplanes. UAL also
suggested adding Model 737–NG
airplanes. AAL stated that the
applicability statement as proposed in
the NPRM could mislead operators into
believing that the AD would apply only
to the airplanes identified in paragraphs
(c)(1) through (12) of the AD. UAL
believed the suggested change will be
beneficial and assist operators in
determining if their fleets are affected.
E:\FR\FM\28FER1.SGM
28FER1
Federal Register / Vol. 87, No. 39 / Monday, February 28, 2022 / Rules and Regulations
The FAA disagrees with the
commenters’ request. The FAA does not
have a comprehensive list of all possible
affected aircraft. To address the
incomplete list, paragraph (c) of this AD
identifies specific airplane models in
paragraph (c) of this AD, but also notes
that the assemblies are ‘‘not limited to.’’
The FAA has not changed the AD in this
regard.
khammond on DSKJM1Z7X2PROD with RULES
Request To Revise Compliance Time for
Parts
AAL stated that the 60-day
compliance time should apply only to
valve assemblies that are installed on
the aircraft and not ones in stock. AAL
believes the unsafe condition only exists
when an assembly is installed on an
airplane, and for those assemblies that
are not installed on an airplane, the
proposed requirements in paragraph (k)
of the proposed AD would ensure that
the unsafe condition is addressed before
that assembly is installed on an aircraft.
The FAA disagrees with the request to
revise the compliance time. The FAA
agrees that an affected spare part that is
uninstalled and stored off an aircraft
would not cause an unsafe condition on
an aircraft. The 60-day compliance time
applies to parts already installed on an
aircraft, and paragraph (k) requires that
action to be done on affected spare parts
before installation, which could result
in a spare part being inspected before
the 60-day compliance time. In
developing the compliance time for this
AD, the FAA considered the urgency
associated with the subject unsafe
condition and the availability of
required parts. The FAA determined
that the 60-day compliance time for
parts already installed on an aircraft is
appropriate for accomplishing the
actions required by this AD while
maintaining an adequate level of safety.
The FAA has not changed this AD in
this regard.
Request To Remove Inspection for
Serial Numbers or Include Only Valve
P/Ns
AAL requested that the inspection to
verify the serial number of the oxygen
cylinder and entire assembly not be
required. DAL requested that paragraphs
(c), (h), (i), and (k) of the proposed AD
be revised to remove reference to
cylinder part numbers (P/Ns) and apply
only to valve assembly P/Ns. AAL stated
that it reviewed the service information
and it seems that the defective part is
only the valve assembly or ‘‘hand
valve.’’ DAL also reasoned that the
unsafe condition applies only to the
valve assembly and not the cylinder.
AAL then reasoned that the inspection
to verify the serial number should apply
VerDate Sep<11>2014
16:12 Feb 25, 2022
Jkt 256001
only to the valve assembly or ‘‘hand
valve.’’ AAL also stated that paragraph
(i) of the proposed AD also seems to
require the actions of paragraph (h)(1)
through (3) of the proposed AD if a
serial number of a cylinder was affected
and a valve assembly not affected, even
though it seems that it should not
require those actions.
The FAA disagrees with the request.
The parts of the oxygen cylinder and
valve assemblies are interrelated, and
valves from matched sets could have fitup issues between parts or be mixed up
or swapped during maintenance
operations. The serial number
inspection as proposed would address
this interchangeability. The valve and
cylinder that are part of those
assemblies must also be inspected to
address the unsafe condition, not just
the assemblies themselves. Therefore,
the FAA specifies to inspect the oxygen
valve assemblies, and oxygen cylinder
and valve assemblies, to determine the
serial number of the valve, cylinder, and
entire assembly. The FAA has not
changed this AD in this regard.
Request To Clarify Which Components
Need To Be Identified
UAL requested a change to the
wording of which components need the
serial number inspection. UAL stated
that the statement in paragraph (h) of
the proposed AD can be misconstrued
as requiring that each of the three
components (valve, cylinder, and entire
assembly) be inspected individually for
suspect serial numbers. UAL inferred
that the intention is to inspect for the
serial number of the entire cylinder and
valve assembly, and not the individual
components. UAL also stated that, for
new oxygen cylinder assemblies from
AVOX, there are individual placards
that itemize the P/N and serial number
for each component, and that for some
cylinder assemblies, the serialization of
the entire cylinder and valve assembly
is nearly identical in format to the
serialization of sub-component valve
assemblies, which could lead to
inaccurate reporting of results. The FAA
infers that UAL suggested that the
relevant numbers on the placards could
be confused with other numbers.
The FAA disagrees. Each part and
assembly stated in paragraph (h) of this
AD are interrelated and must be
inspected. The valve and cylinder
components that are part of those
assemblies must also be inspected for
serial numbers, not just the assemblies
themselves. If the serial number
markings are unclear or missing, the
service information contains
information on identifying the parts and
PO 00000
Frm 00035
Fmt 4700
Sfmt 4700
10959
part assemblies. The FAA has not
changed this AD in this regard.
Request To Revise Conditions for Gap
Inspection and Related Actions
AAL and DAL requested changes to
address concerns about what actions are
required if a part is missing a blue dot.
DAL stated that it seems best to prohibit
all affected serial numbers to avoid a
case where an inspected and marked
part is installed, but the blue dot fades.
AAL pointed to paragraph (i) of the
proposed AD that would clarify that
only the affected serial numbers of the
valve assembly would need additional
work, and, for valve assemblies marked
with a blue dot, a detailed inspection for
correct spacing of the gap between the
bottom of the packing retainer and top
of the valve body would not be required.
AAL stated that, as written, the
proposed AD seems to suggest that an
inspection of the gap would be required
regardless of the presence of a blue dot.
The FAA disagrees with the request.
The service information specifies that if
there is a doubt on the condition of a
part, such as missing serial numbers or
a blue dot not definitively identified,
then the follow-on inspections are
required to ensure that no discrepant or
affected part is missed. Paragraph (k) of
this AD prohibits installation of
assemblies with affected serial numbers
unless the actions of paragraph (i) of
this AD are accomplished. The FAA has
not changed this AD in this regard.
Request To Remove Inspection Report
Requirement
DAL requested that the compliance
times for the inspection report be
removed from paragraph (j)(1) of the
proposed NPRM, and if not, the
inspection report itself be removed.
AAL requested removing the proposed
requirement to submit an inspection
report after accomplishing the
requirements (i.e., gap inspection) of
paragraph (i) of the proposed AD. FedEx
stated reporting should not be required
for units that pass the inspection, and
that sending units that failed the
inspection to the vendor should be
sufficient for reporting those failures.
FedEx noted that any reporting
requirements should consider the
difficulties in reporting findings in a
short period of time and noted that the
inspector might not have access to the
internet, email, and a device capable of
printing and scanning. FedEx opined
that its proposal would maintain
accurate reporting and accommodate the
realities of a global workplace. AAL and
DAL stated that the reporting seems
unnecessary and does not contribute to
any additional level of safety. AAL
E:\FR\FM\28FER1.SGM
28FER1
10960
Federal Register / Vol. 87, No. 39 / Monday, February 28, 2022 / Rules and Regulations
khammond on DSKJM1Z7X2PROD with RULES
added that the NPRM would give
operators the responsibility of ensuring
that any affected part is returned to the
manufacturer, and asserted that an
equivalent level of safety would be
maintained even if the reporting is not
accomplished. DAL reasoned that if a
cylinder valve assembly is
unacceptable, it would be in the
operator’s best interest to report that
finding to AVOX anyways so that it can
receive a replacement assembly.
The FAA disagrees. In this case, the
inspection results need to be reported to
assist in tracking affected parts that are
in circulation. In addition, reporting all
findings gives assurance that an
inspection was performed on an
assembly with a given serial number.
The FAA has not changed this AD in
this regard.
Request To Remove Compliance Time
for Returning Parts
AAL, DAL, and UAL requested
revising paragraph (j)(2) of the proposed
AD to remove a compliance time for
returning discrepant parts to the
manufacturer. AAL stated that a
compliance time would not contribute
to the level of safety. AAL also stated
that all discrepant assemblies would be
returned in a timely manner that is
sufficient to the operator. DAL stated
that it would be an unnecessary burden
on operators to wait for AVOX’s
response before sending an
unacceptable or discrepant part back
within the compliance time in exchange
for a free-of-charge replacement. DAL
also stated that it would also be in the
operator’s best interest to send in the
assembly so that it can qualify for a freeof-charge replacement if AVOX
determines the part is unacceptable or
discrepant. UAL stated it also believes
the instruction to contact AVOX for
shipping instructions could impede
compliance with the 30-day limit to
ship discrepant parts back to AVOX.
UAL also stated that it wants to know
how, for accurate AD-compliance
reporting, it would be determined that
a part is being shipped back as a result
of this finding from AD-required
inspections, or as a result of other,
normal repair order processes.
The FAA agrees to clarify. Paragraph
(j)(2) of this AD requires returning the
assembly to the manufacturer in
accordance with paragraph 3.D.(2) or
3.D.(3), as applicable, of the applicable
service information. However, the
service information does not include
instructions to wait for a response from
AVOX before returning the part. In
addition, the FAA has revised paragraph
(j)(2) of this AD to clarify that contacting
AVOX for shipping instructions in not
VerDate Sep<11>2014
16:12 Feb 25, 2022
Jkt 256001
required. AVOX is tracking parts that
are returned to it during
accomplishment of the AD for data
collection or analysis of manufacturing
issues, and AVOX is also reconditioning parts where possible. The
FAA determined that having a 30-day
compliance time for returning the part
after an inspection finding is
appropriate for this AD. However, under
the provisions of paragraph (m) of this
AD, an operator may request an
approval of an alternative method of
compliance (AMOC). The FAA has not
changed this AD in this regard.
The FAA disagrees. The definition of
the affected units does not need to be
moved to paragraph (c) of the AD. The
effectivity of the service information is
limited to specific airplane models, but
the applicability of this AD applies to
all aircraft. Because the affected parts
could be installed on additional aircraft
models, the FAA has determined that
the affected parts could later be
installed on aircraft that were initially
delivered with acceptable parts, thereby
subjecting those aircraft to the unsafe
condition. The FAA has not changed
this AD in this regard.
Request To Allow Later Revisions of
Service Information
AAL requested that all the references
to the AVOX service information be
revised to allow use of subsequent
revisions. AAL reasoned that this
revision would reduce the number of
AMOC requests each time a referenced
service bulletin is revised.
The FAA disagrees. In an AD, the
FAA may not refer to any document that
does not yet exist. In general terms, the
FAA is required by the Office of the
Federal Register (OFR) regulations for
approval of materials incorporated by
reference, as specified in 1 CFR 51.1(f),
to either publish the service document
contents as part of the actual AD
language; or submit the service
document to the OFR for approval as
referenced material, in which case the
FAA may only refer to such material in
the text of an AD. The AD may refer to
the service document only if the OFR
approved it for incorporation by
reference. See 1 CFR part 51. The FAA
disagrees with revising the AD to
include specific airplane models based
on the corresponding service
information because the agency does not
have a comprehensive list of the
applicable aircraft to which specific
AVOX service information could apply.
The FAA has not changed this AD in
this regard.
Request To Revise Compliance Time for
Parts Identification
DAL and UAL requested revising the
compliance time proposed in paragraph
(h) of the proposed NPRM. DAL and
UAL stated that since many operators
have parked their aircraft or severely
reduced usage of aircraft, an extension
of the compliance time (either with
additional calendar days or adding an
option for flight hours and flight cycles),
would allow operators additional time
for compliance. UAL also stated that the
supply chain could be affected due to
potential increased shipping time and
workforce reductions.
The FAA disagrees with the request to
extend the compliance time. The FAA
acknowledges the effects that the
pandemic response might have on
operators’ fleet use, supply chain, and
maintenance personnel. In developing
an appropriate compliance time for this
action, the FAA considered the degree
of urgency associated with addressing
the subject unsafe condition, the
manufacturer’s recommendation for an
appropriate compliance time, and the
practical aspect of accomplishing the
required inspection within a period of
time that corresponds to the normal
scheduled maintenance for most
affected operators. In addition, the FAA
notes that some aircraft may have been
in service during the pandemic and
must comply within the required
compliance time. Operators do have the
option to inspect the airplane before the
first flight following storage if the
airplane is in storage for more than 27
months. However, under the provisions
of paragraph (m) of this AD, the FAA
will consider requests for an extension
of the compliance time if sufficient data
are submitted to substantiate that the
new compliance time would provide an
acceptable level of safety. The FAA has
not changed this AD in this regard.
Request To Clarify AD Applicability
With Reference to Service Information
A commenter requested clarifying
paragraph (c) of the proposed AD by
including reference to the service
information that was identified in
paragraph (h) of the proposed AD. The
commenter suggested revising the
paragraph so that the applicability
would include information on the
service information definition of the
affected units. AAL also requested
adding the airplane configuration
information in the text of the AD to add
further clarification to operators and
release the technical data in a more
organized fashion.
PO 00000
Frm 00036
Fmt 4700
Sfmt 4700
Request To Allow Use of Alternatives
for Parts Marking
FedEx requested that the specification
to use oil-based blue ink markers be
E:\FR\FM\28FER1.SGM
28FER1
Federal Register / Vol. 87, No. 39 / Monday, February 28, 2022 / Rules and Regulations
modified to allow alternative methods
and colors such as black indelible ink.
FedEx stated that oil-based blue paint
markers are not readily available or kept
in stock regularly. FedEx suggested that
a list of part numbers for approved,
aircraft grade, oil-based paint be
provided.
The FAA disagrees. While the FAA
realizes this is a limitation, there must
be one standard to help avoid
confusion. The procedures required by
this AD specify actions based on the
presence or absence of a blue dot in a
specific location. The FAA has not seen
any difficulties in obtaining the paint
markers. However, under the provisions
of paragraph (m) of this AD, any person
may request an approval of an AMOC.
The FAA has not revised this AD in this
regard.
khammond on DSKJM1Z7X2PROD with RULES
Request To Allow Alternative Means of
Measuring Gaps
FedEx requested that the proposed
AD be revised to allow use of feeler
gauges, calipers, and other means of
measuring the gap in imperial units of
measure. FedEx stated that the service
information specifies use of pin gauges
that are made for metric units of
measure, and that acquiring those
metric pin gauges is an extra expense
and logistical complication. FedEx
recommended adding a tolerance to the
gap measurement and specifying a
fractional imperial measure (3⁄32-inch)
that is close to the metric unit specified.
FedEx suggested that if a tolerance or
other measurement is not added, then a
manufacturer part number (MPN) for a
specific tool or supplier should be
provided.
The FAA disagrees. Using other
means of measuring could introduce or
increase variables that could affect the
accuracy of the measurement. The FAA
understands that not everyone has the
same resources, tools, or supplies;
however, the FAA also understands that
this means of measurement is easily
accessible. Under the provisions of
paragraph (m) of this AD, operators may
request approval of an AMOC if
sufficient data are submitted to
substantiate that the tolerance would
provide an acceptable level of safety.
The FAA has not changed this AD in
this regard.
Request To Revise Procedure for
Shipping an Assembly
FedEx requested that the proposed
AD be revised to allow operators to use
their own procedures for shipping
dangerous goods such as unopened
cylinder valve assemblies (CVAs)
instead of the procedure specified in the
service information. FedEx explained
VerDate Sep<11>2014
16:12 Feb 25, 2022
Jkt 256001
that it has established and accepted
procedures for shipping dangerous
goods, and that the disposition of an
unopened CVA would be done by a
department separate from the one doing
the inspection. FedEx stated that
following the procedures in the service
information would require additional
coordination time, and that the wording
of the procedures would not function
properly with its AD compliance
mechanisms.
The FAA agrees to clarify. The design
approval holder (DAH) of the affected
valve assemblies has specified a method
for shipping, or returning, an unopened
CVA that has been found to be
unacceptable or discrepant, specifically
a shipping method that is compliant
with DOT standard HM–224B. If FedEx
has procedures that are compliant with
DOT standard HM–224B, then those
procedures are acceptable for
compliance with this AD. For
procedures that are not compliant with
DOT standard HM–224B, under the
provisions of paragraph (m) of this AD,
the FAA will consider requests for an
AMOC. The FAA has not changed this
AD in this regard.
Request for Clarification on
Applicability of AD
FedEx requested clarification on
whether the proposed AD is written
‘‘against’’ the MPN or the serial numbers
within that MPN. FedEx explained the
effects on the operator’s workload and
also on the operational impact of a
unit’s overhaul cycle in conjunction
with a 60-day compliance time and the
scope of the applicability. FedEx added
that a 180-day compliance time would
be more reasonable.
The FAA agrees to clarify. The
applicability of this AD is written
against the MPN and specific serial
numbers, in addition to manufacture
dates of the assemblies. The FAA
disagrees to revise the compliance time
because the FAA has determined that
requirement based on a risk calculation.
The FAA has not changed this AD in
that regard.
Request To Clarify Requirement if
Component Number(s) Cannot Be
Determined
UAL requested clarification on what
actions are required in the event the
P/N or serial number information
cannot be determined. UAL stated that
as a result of in-service activity, that
information might be illegible,
unintentionally obliterated, or missing
from the placard. UAL added that under
its normal practices, whenever a part or
serial number cannot be determined, the
part is considered suspect, made
PO 00000
Frm 00037
Fmt 4700
Sfmt 4700
10961
unserviceable, and removed from
service. UAL stated that, when the P/N
of the entire cylinder and valve
assembly can be determined but not the
serial number, and the date of
manufacture is between January and
November 2018, it wants to still be able
to establish conformity by inspecting for
the presence of the blue dot and
accomplish the applicable service
information instruction if the blue dot is
missing. UAL also stated that depending
on the FAA’s response to this request,
it may apply for an AMOC.
The FAA agrees to clarify. The service
information states to inspect for the
manufacturing date, serial number, and
the presence of a blue dot. The service
information then states that if there is
doubt or a determination cannot be
made (such as the numbers or dot is not
clearly identified), to proceed with the
follow-on inspection for proper gap
spacing (this follow-on inspection is
required by paragraph (i) of this AD).
The FAA has not changed this AD in
this regard.
Request for Clarification on
Compliance Time and Method for
Inspection Report
UAL requested clarification on how a
30-day requirement for the inspection
report was determined, and if a
‘‘comprehensive’’ report is acceptable.
UAL stated that it understands the need
for the information gathered from the
reports; however, it does not understand
why or how a 30-day compliance time
was established. UAL also stated that it
assumed that reporting of the results
should be done as a single,
comprehensive report and not piecewise (individually for each assembly or
aircraft), and that the report does not
need to be an exact copy of the report
form in the service information.
The FAA agrees to clarify. The FAA
determined that the 30-day compliance
time is appropriate for this AD. Also,
the manufacturer is collecting
information for analysis of
manufacturing issues. The format of the
report may be done as UAL assumed, as
long as all documents are labeled
correctly. However, under the
provisions of paragraph (m) of this AD,
an operator may request an approval of
an AMOC. The FAA has not changed
this AD in this regard.
Request To Provide Clarification on
Reporting Form
UAL requested clarification on the
definition of ‘‘manufacture date’’ in a
recording column of a report form in the
service information. UAL stated that it
is implied that ‘‘manufacture date’’ in
that column is the manufacture date of
E:\FR\FM\28FER1.SGM
28FER1
10962
Federal Register / Vol. 87, No. 39 / Monday, February 28, 2022 / Rules and Regulations
the entire cylinder and valve assembly
and not of the valve assembly.
The FAA agrees to clarify. The
‘‘manufacturer date’’ is not limited to
the date of the entire cylinder and valve
assembly, but is the manufacture date of
each part or assembly that might be
recorded in the inspection report, such
as the assemblies listed in Appendix 1
of the service information. The FAA has
not changed this AD in this regard.
Conclusion
The FAA reviewed the relevant data,
considered any comments received, and
determined that air safety requires
adopting this AD as proposed. Except
for minor editorial changes, this AD is
adopted as proposed in the NPRM.
None of the changes will increase the
economic burden on any operator.
Related Service Information Under 1
CFR Part 51
The FAA reviewed AVOX Systems
Inc. Alert Service Bulletins 10015804–
35–01, Revision 02, dated October 16,
2019; 10015804–35–02, Revision 2,
dated October 31, 2019; and 10015804–
35–03, Revision 02, dated October 15,
2019. This service information describes
procedures for an inspection to
determine the serial numbers of the
oxygen cylinder and valve assemblies,
and the oxygen valve assemblies, a
detailed inspection for correct spacing
of the gap between the bottom of the
packing retainer and top of the valve
body on the assemblies, parts marking,
inspection report, and return of parts to
the manufacturer. These documents are
distinct since they apply to different
assembly part numbers. This service
information is reasonably available
because the interested parties have
access to it through their normal course
of business or by the means identified
in ADDRESSES.
Costs of Compliance
The FAA estimates that this AD
affects up to 3,034 oxygen cylinder and
valve assemblies, and oxygen valve
assemblies, installed on various
transport category airplanes of U.S.
registry. The FAA estimates the
following costs to comply with this AD:
ESTIMATED COSTS
Action
Labor cost
Parts cost
Serial number inspection ...............................
Reporting .......................................................
1 work-hour × $85 per hour = $85 ...............
1 work-hour × $85 per hour = $85 ...............
None .................
0 .......................
The FAA estimates the following
costs to do any necessary follow-on
actions that would be required based on
the results of the inspection. The FAA
Cost per
product
$85
85
Cost on U.S.
operators
$257,890
257,890
has no way of determining the number
of aircraft that might need these actions:
ON-CONDITION COSTS *
Action
Labor cost
Parts cost
Detailed inspection ......................................................
1 work-hour × $85 per hour = $85 .............................
None .................
Cost per
product
$85
* The FAA has received no definitive data on the cost of on-condition replacements.
According to the manufacturer, some
or all of the costs of this AD may be
covered under warranty, thereby
reducing the cost impact on affected
operators. The FAA does not control
warranty coverage for affected operators.
As a result, the FAA has included all
known costs in the cost estimate.
khammond on DSKJM1Z7X2PROD with RULES
Paperwork Reduction Act
A federal agency may not conduct or
sponsor, and a person is not required to
respond to, nor shall a person be subject
to a penalty for failure to comply with
a collection of information subject to the
requirements of the Paperwork
Reduction Act unless that collection of
information displays a currently valid
OMB Control Number. The OMB
Control Number for this information
collection is 2120–0056. Public
reporting for this collection of
information is estimated to take
approximately 1 hour per response,
including the time for reviewing
instructions, searching existing data
sources, gathering and maintaining the
data needed, and completing and
VerDate Sep<11>2014
16:12 Feb 25, 2022
Jkt 256001
reviewing the collection of information.
All responses to this collection of
information are mandatory. Send
comments regarding this burden
estimate or any other aspect of this
collection of information, including
suggestions for reducing this burden to:
Information Collection Clearance
Officer, Federal Aviation
Administration, 10101 Hillwood
Parkway, Fort Worth, TX 76177–1524.
Authority for This Rulemaking
Title 49 of the United States Code
specifies the FAA’s authority to issue
rules on aviation safety. Subtitle I,
section 106, describes the authority of
the FAA Administrator. Subtitle VII:
Aviation Programs, describes in more
detail the scope of the Agency’s
authority.
The FAA is issuing this rulemaking
under the authority described in
Subtitle VII, Part A, Subpart III, Section
44701: General requirements. Under
that section, Congress charges the FAA
with promoting safe flight of civil
aircraft in air commerce by prescribing
PO 00000
Frm 00038
Fmt 4700
Sfmt 4700
regulations for practices, methods, and
procedures the Administrator finds
necessary for safety in air commerce.
This regulation is within the scope of
that authority because it addresses an
unsafe condition that is likely to exist or
develop on products identified in this
rulemaking action.
Regulatory Findings
This AD will not have federalism
implications under Executive Order
13132. This AD will not have a
substantial direct effect on the States, on
the relationship between the national
government and the States, or on the
distribution of power and
responsibilities among the various
levels of government.
For the reasons discussed above, I
certify that this AD:
(1) Is not a ‘‘significant regulatory
action’’ under Executive Order 12866,
(2) Will not affect intrastate aviation
in Alaska, and
(3) Will not have a significant
economic impact, positive or negative,
on a substantial number of small entities
E:\FR\FM\28FER1.SGM
28FER1
Federal Register / Vol. 87, No. 39 / Monday, February 28, 2022 / Rules and Regulations
under the criteria of the Regulatory
Flexibility Act.
List of Subjects in 14 CFR Part 39
Air transportation, Aircraft, Aviation
safety, Incorporation by reference,
Safety.
The Amendment
Accordingly, under the authority
delegated to me by the Administrator,
the FAA amends 14 CFR part 39 as
follows:
(d) Subject
Air Transport Association (ATA) of
America Code 35, Oxygen System.
PART 39—AIRWORTHINESS
DIRECTIVES
1. The authority citation for part 39
continues to read as follows:
■
Authority: 49 U.S.C. 106(g), 40113, 44701.
§ 39.13
[Amended]
2. The FAA amends § 39.13 by adding
the following new airworthiness
directive:
■
2022–04–09 AVOX Systems Inc. (formerly
Scott Aviation): Amendment 39–21951;
Docket No. FAA–2020–0345; Product
Identifier 2019–NM–154–AD.
(a) Effective Date
This airworthiness directive (AD) is
effective April 4, 2022.
khammond on DSKJM1Z7X2PROD with RULES
(b) Affected ADs
None.
(c) Applicability
This AD applies to AVOX Systems Inc.
(formerly Scott Aviation) oxygen cylinder
and valve assemblies having part number
(P/N) 89794077, 89794015, 891511–14,
806835–01, 807982–01, or 808433–01; and
oxygen valve assemblies (body and gage
assemblies) having P/N 807206–01. These
assemblies might be installed on, but not
limited to, the aircraft identified in
paragraphs (c)(1) through (12) of this AD,
certificated in any category.
(1) Airbus SAS Model A300 B2–1A, B2–
1C, B2K–3C, B2–203, B4–2C, B4–103, and
B4–203 airplanes.
(2) Airbus SAS Model A300 B4–601, B4–
603, B4–620, B4–622, B4–605R, B4–622R,
F4–605R, F4–622R, and C4–605R Variant F
airplanes.
(3) Airbus SAS Model A310–203, –204,
–221, –222, –304, –322, –324, and –325
airplanes.
(4) Airbus SAS Model A318–111, –112,
–121, and –122 airplanes.
(5) Airbus SAS Model A319–111, –112,
–113, –114, –115, –131, –132, –133, and
–151N airplanes.
(6) Airbus SAS Model A320–211, –212,
–214, –216, –231, –232, –233, –251N, –252N,
–253N, –271N, –272N, and –273N airplanes.
(7) Airbus SAS Model A321–111, –112,
–131, –211, –212, –213, –231, –232, –251N,
–252N, –253N, –271N, –272N, –251NX,
–252NX, –253NX, –271NX, and –272NX
airplanes.
(8) Airbus SAS Model A330–201, –202,
–203, –223, –243, –301, –302, –303, –321,
VerDate Sep<11>2014
16:12 Feb 25, 2022
Jkt 256001
–322, –323, –341, –342, –343, and –941
airplanes.
(9) Airbus Model A340–211, –212, –213,
–311, –312, –313, –541, and –642 airplanes.
(10) ATR—GIE Avions de Transport
Re´gional Model ATR42–200, –300, –320, and
–500 airplanes.
(11) ATR—GIE Avions de Transport
Re´gional Model ATR72–101, –102, –201,
–202, –211, –212, and –212A airplanes.
(12) The Boeing Company Model 747–8
series airplanes.
(e) Unsafe Condition
This AD was prompted by reports of
cylinder and valve assemblies having oxygen
leakage from the valve assembly vent hole,
caused by the absence of a guide that
maintains appropriate spacing between
certain parts. The FAA is issuing this AD to
address oxygen leakage from the cylinder,
which could result in decreased or
insufficient oxygen supply during a
depressurization event; and heating or flow
friction, which could cause an ignition event
in the valve assembly.
(f) Compliance
Comply with this AD within the
compliance times specified, unless already
done.
(g) Definition of Detailed Inspection
For the purposes of this AD, a detailed
inspection is an intensive examination of a
specific item, installation, or assembly to
detect damage, failure, or irregularity.
Available lighting is normally supplemented
with a direct source of good lighting at an
intensity deemed appropriate. Inspection
aids such as mirror, magnifying lenses, etc.,
may be necessary. Surface cleaning and
elaborate procedures may be required.
(h) Identification of Affected Cylinder and
Valve Assemblies
Within 60 days after the effective date of
this AD, inspect the oxygen valve assemblies,
and oxygen cylinder and valve assemblies, to
determine if the serial numbers of the valve,
cylinder, and entire assembly, are listed in
Appendix 1, ‘‘Affected Shipments,’’ of the
applicable service information identified in
paragraphs (h)(1) through (3) of this AD. A
review of airplane maintenance records is
acceptable in lieu of this inspection if the
serial numbers can be conclusively
determined from that review.
(1) AVOX Systems Inc. Alert Service
Bulletin 10015804–35–01, Revision 02, dated
October 16, 2019.
(2) AVOX Systems Inc. Alert Service
Bulletin 10015804–35–02, Revision 2, dated
October 31, 2019.
(3) AVOX Systems Inc. Alert Service
Bulletin 10015804–35–03, Revision 02, dated
October 15, 2019.
(i) Inspection of the Gap, Parts Marking
Actions, and Replacement
If, during any inspection or records review
required by paragraph (h) of this AD, any
oxygen valve assembly, valve or cylinder of
PO 00000
Frm 00039
Fmt 4700
Sfmt 4700
10963
an oxygen cylinder and valve assembly, or
oxygen cylinder and valve assembly having
an affected serial number is found: Before
further flight, do a detailed inspection for
correct spacing of the gap between the
bottom of the packing retainer and top of the
valve body, in accordance with paragraph
3.C. of the Accomplishment Instructions of
the applicable service information identified
in paragraphs (h)(1) through (3) of this AD.
(1) If the gap is found to be acceptable, as
defined in the applicable service information
identified in paragraphs (h)(1) through (3) of
this AD, before further flight, do the parts
marking actions in accordance with
paragraph 3.D.(1) of the Accomplishment
Instructions of the applicable service
information identified in paragraphs (h)(1)
through (3) of this AD.
(2) If the gap is found to be unacceptable,
as defined in the applicable service
information identified in paragraphs (h)(1)
through (3) of this AD, before further flight,
remove the affected assembly, in accordance
with paragraphs 3.D.(2) or 3.D.(3), as
applicable, of the Accomplishment
Instructions of the applicable service
information identified in paragraphs (h)(1)
through (3) of this AD; and replace with a
serviceable assembly.
(j) Reporting and Return of Parts
(1) Report the results of the inspection
required by paragraph (i) of this AD within
the applicable time specified in paragraph
(j)(1)(i) or (ii) of this AD. Report the results
in accordance with paragraph 3.D.(1)(a) of
the Accomplishment Instructions of the
applicable service information identified in
paragraphs (h)(1) through (3) of this AD.
(i) If the inspection was done on or after
the effective date of this AD: Submit the
report within 30 days after the inspection.
(ii) If the inspection was done before the
effective date of this AD: Submit the report
within 30 days after the effective date of this
AD.
(2) If, during the inspection required by
paragraph (i) of this AD, any gap is found to
be unacceptable, within the applicable time
specified in paragraph (j)(2)(i) or (ii) of this
AD, return the assembly to the manufacturer
in accordance with paragraph 3.D.(2) or
3.D.(3), as applicable, of the Accomplishment
Instructions of the applicable service
information identified in paragraphs (h)(1)
through (3) of this AD, except you are not
required to contact AVOX for shipping
instructions.
(i) If the inspection was done on or after
the effective date of this AD: Return the
assembly within 30 days after the inspection.
(ii) If the inspection was done before the
effective date of this AD: Return the assembly
within 30 days after the effective date of this
AD.
(k) Parts Installation Limitation
As of the effective date of this AD, no
AVOX Systems Inc. oxygen valve assembly,
or valve or cylinder that is part of an oxygen
cylinder and valve assembly, or oxygen
cylinder and valve assembly having an
affected serial number identified in
Appendix 1, ‘‘Affected Shipments,’’ of any
AVOX Systems Inc. service information
E:\FR\FM\28FER1.SGM
28FER1
10964
Federal Register / Vol. 87, No. 39 / Monday, February 28, 2022 / Rules and Regulations
identified in paragraphs (h)(1) through (3) of
this AD may be installed on any airplane
unless the requirements of paragraph (i) of
this AD have been accomplished on that
affected assembly.
(l) Credit for Previous Actions
This paragraph provides credit for the
actions specified in paragraphs (h) or (i) of
this AD, if those actions were performed
before the effective date of this AD using the
service information specified in paragraphs
(l)(1) through (5) of this AD.
(1) AVOX Systems Inc. Service Bulletin
10015804–35–01, dated March 6, 2019.
(2) AVOX Systems Inc. Alert Service
Bulletin 10015804–35–01, Revision 01, dated
July 9, 2019.
(3) AVOX Systems Inc. Alert Service
Bulletin 10015804–35–02, Revision 1, dated
September 4, 2019.
(4) AVOX Systems Inc. Service Bulletin
10015804–35–03, dated April 11, 2019.
(5) AVOX Systems Inc. Alert Service
Bulletin 10015804–35–03, Revision 01, dated
May 21, 2019.
(m) Alternative Methods of Compliance
(AMOCs)
(1) The Manager, New York ACO Branch,
FAA, has the authority to approve AMOCs
for this AD, if requested using the procedures
found in 14 CFR 39.19. In accordance with
14 CFR 39.19, send your request to your
principal inspector or local Flight Standards
District Office, as appropriate. If sending
information directly to the manager of the
certification office, send it to ATTN: Program
Manager, Continuing Operational Safety,
FAA, New York ACO Branch, 1600 Stewart
Avenue, Suite 410, Westbury, NY 11590;
telephone 516–228–7300; fax 516–794–5531.
(2) Before using any approved AMOC,
notify your appropriate principal inspector,
or lacking a principal inspector, the manager
of the local flight standards district office/
certificate holding district office.
Issued on February 11, 2022.
Lance T. Gant,
Director, Compliance & Airworthiness
Division, Aircraft Certification Service.
(n) Related Information
[Docket No. FDA–2021–N–0002]
(1) For more information about this AD,
contact Elizabeth Dowling, Aerospace
Engineer, Mechanical Systems and
Administrative Services Section, FAA, New
York ACO Branch, 1600 Stewart Avenue,
Suite 410, Westbury, NY 11590; telephone
516–228–7300; email 9-avs-nyaco-cos@
faa.gov.
(2) Service information identified in this
AD that is not incorporated by reference is
available at the addresses specified in
paragraphs (o)(3) and (4) of this AD.
New Animal Drugs; Approval of New
Animal Drug Applications; Withdrawal
of Approval of a New Animal Drug
Application; Change of Sponsor
(o) Material Incorporated by Reference
khammond on DSKJM1Z7X2PROD with RULES
(i) AVOX Systems Inc. Alert Service
Bulletin 10015804–35–01, Revision 02, dated
October 16, 2019.
(ii) AVOX Systems Inc. Alert Service
Bulletin 10015804–35–02, Revision 2, dated
October 31, 2019.
(iii) AVOX Systems Inc. Alert Service
Bulletin 10015804–35–03, Revision 02, dated
October 15, 2019.
(3) For service information identified in
this AD, contact AVOX Systems Inc., 225
Erie Street, Lancaster, NY 14086; telephone
716–683–5100; internet https://
www.safranaerosystems.com.
(4) You may view this service information
at the FAA, Airworthiness Products Section,
Operational Safety Branch, 2200 South 216th
St., Des Moines, WA. For information on the
availability of this material at the FAA, call
206–231–3195.
(5) You may view this service information
that is incorporated by reference at the
National Archives and Records
Administration (NARA). For information on
the availability of this material at NARA,
fr.inspection@nara.gov, or go to: https://
www.archives.gov/federal-register/cfr/ibrlocations.html.
(1) The Director of the Federal Register
approved the incorporation by reference
(IBR) of the service information listed in this
paragraph under 5 U.S.C. 552(a) and 1 CFR
part 51.
(2) You must use this service information
as applicable to do the actions required by
this AD, unless the AD specifies otherwise.
VerDate Sep<11>2014
16:12 Feb 25, 2022
Jkt 256001
[FR Doc. 2022–04146 Filed 2–25–22; 8:45 am]
BILLING CODE 4910–13–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
21 CFR Parts 500, 510, 516, 520, 522,
524, 529, 556, and 558
AGENCY:
Food and Drug Administration,
HHS.
Final rule; technical
amendments.
ACTION:
The Food and Drug
Administration (FDA or we) is
amending the animal drug regulations to
reflect application-related actions for
new animal drug applications (NADAs),
abbreviated new animal drug
applications (ANADAs), and a
conditionally approved new animal
drug application (cNADA) during July,
August, and September 2021. FDA is
SUMMARY:
PO 00000
Frm 00040
Fmt 4700
Sfmt 4700
informing the public of the availability
of summaries of the basis of approval
and of environmental review
documents, where applicable. The
animal drug regulations are also being
amended to improve the accuracy of the
regulations.
This rule is effective February
28, 2022. The incorporation by reference
of certain material listed in this rule is
approved by the Director of the Federal
Register as February 28, 2022. The
incorporation by reference of other
material listed in this rule was approved
by the Director of the Federal Register
as of November 25, 2011.
DATES:
FOR FURTHER INFORMATION CONTACT:
George K. Haibel, Center for Veterinary
Medicine (HFV–6), Food and Drug
Administration, 7500 Standish Pl.,
Rockville, MD 20855, 240–402–5689,
george.haibel@fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Approvals
FDA is amending the animal drug
regulations to reflect approval actions
for NADAs and ANADAs during July,
August, and September 2021, as listed
in table 1. In addition, FDA is informing
the public of the availability, where
applicable, of documentation of
environmental review required under
the National Environmental Policy Act
(NEPA) and, for actions requiring
review of safety or effectiveness data,
summaries of the basis of approval (FOI
Summaries) under the Freedom of
Information Act (FOIA). These public
documents may be seen in the office of
the Dockets Management Staff (HFA–
305), Food and Drug Administration,
5630 Fishers Lane, Rm. 1061, Rockville,
MD 20852, between 9 a.m. and 4 p.m.,
Monday through Friday, 240–402–7500.
Persons with access to the internet may
obtain these documents at the CVM
FOIA Electronic Reading Room: https://
www.fda.gov/about-fda/centerveterinary-medicine/cvm-foiaelectronic-reading-room. Marketing
exclusivity and patent information may
be accessed in FDA’s publication,
‘‘Approved Animal Drug Products
Online (Green Book)’’ at: https://
www.fda.gov/animal-veterinary/
products/approved-animal-drugproducts-green-book.
FDA has verified the website
addresses as of the date this document
publishes in the Federal Register, but
websites are subject to change over time.
E:\FR\FM\28FER1.SGM
28FER1
Agencies
[Federal Register Volume 87, Number 39 (Monday, February 28, 2022)]
[Rules and Regulations]
[Pages 10958-10964]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-04146]
-----------------------------------------------------------------------
DEPARTMENT OF TRANSPORTATION
Federal Aviation Administration
14 CFR Part 39
[Docket No. FAA-2020-0345; Product Identifier 2019-NM-154-AD; Amendment
39-21951; AD 2022-04-09]
RIN 2120-AA64
Airworthiness Directives; AVOX System Inc. (Formerly Scott
Aviation) Oxygen Cylinder and Valve Assemblies and Oxygen Valve
Assemblies
AGENCY: Federal Aviation Administration (FAA), DOT.
ACTION: Final rule.
-----------------------------------------------------------------------
SUMMARY: The FAA is adopting a new airworthiness directive (AD) for
certain AVOX System Inc. (formerly Scott Aviation) oxygen cylinder and
valve assemblies, and oxygen valve assemblies, installed on but not
limited to various transport airplanes. This AD was prompted by reports
of cylinder and valve assemblies having oxygen leakage from the valve
assembly vent hole, caused by the absence of a guide that maintains
appropriate spacing between certain parts. This AD requires an
inspection of the oxygen valve assemblies, and oxygen cylinder and
valve assemblies, to determine the serial number of the valve,
cylinder, and entire assembly. For assemblies and parts with certain
serial numbers, this AD requires a detailed inspection for correct
spacing of the gap between the bottom of the packing retainer and top
of the valve body on the assemblies, and replacement of assemblies
having unacceptable gaps. The FAA is issuing this AD to address the
unsafe condition on these products.
DATES: This AD is effective April 4, 2022.
The Director of the Federal Register approved the incorporation by
reference of certain publications listed in this AD as of April 4,
2022.
ADDRESSES: For service information identified in this final rule,
contact AVOX Systems Inc., 225 Erie Street, Lancaster, NY 14086;
telephone 716-683-5100; internet https://www.safranaerosystems.com. You
may view this service information at the FAA, Airworthiness Products
Section, Operational Safety Branch, 2200 South 216th St., Des Moines,
WA. For information on the availability of this material at the FAA,
call 206-231-3195. It is also available at https://www.regulations.gov
by searching for and locating Docket No. FAA-2020-0345.
Examining the AD Docket
You may examine the AD docket at https://www.regulations.gov by
searching for and locating Docket No. FAA-2020-0345; or in person at
Docket Operations between 9 a.m. and 5 p.m., Monday through Friday,
except Federal holidays. The AD docket contains this final rule, any
comments received, and other information. The address for Docket
Operations is U.S. Department of Transportation, Docket Operations, M-
30, West Building Ground Floor, Room W12-140, 1200 New Jersey Avenue
SE, Washington, DC 20590.
FOR FURTHER INFORMATION CONTACT: Elizabeth Dowling, Aerospace Engineer,
Mechanical Systems and Administrative Services Section, FAA, New York
ACO Branch, 1600 Stewart Avenue, Suite 410, Westbury, NY 11590;
telephone 516-228-7300; email [email protected].
SUPPLEMENTARY INFORMATION:
Background
The FAA issued a notice of proposed rulemaking (NPRM) to amend 14
CFR part 39 by adding an AD that would apply to certain AVOX System
Inc. (formerly Scott Aviation) oxygen cylinder and valve assemblies,
and oxygen valve assemblies, installed on but not limited to various
transport airplanes. The NPRM published in the Federal Register on May
1, 2020 (85 FR 25353). The NPRM was prompted by reports of cylinder and
valve assemblies having oxygen leakage from the valve assembly vent
hole, caused by the absence of a guide that maintains appropriate
spacing between certain parts. In the NPRM, the FAA proposed to require
an inspection of the oxygen valve assemblies, and oxygen cylinder and
valve assemblies, to determine the serial number of the valve,
cylinder, and entire assembly. For assemblies and parts with certain
serial numbers, the NPRM proposed to require a detailed inspection for
correct spacing of the gap between the bottom of the packing retainer
and top of the valve body on the assemblies, and replacement of
assemblies having unacceptable gaps (removing affected assemblies and
installing serviceable assemblies). The NPRM also proposed to require
reporting and returning of affected parts to the manufacturer. The FAA
is issuing this AD to address oxygen leakage from the cylinder, which
could result in decreased or insufficient oxygen supply during a
depressurization event; and heating or flow friction, which could cause
an ignition event in the valve assembly.
Discussion of Final Airworthiness Directive
Comments
The FAA received comments from one commenter, Air Line Pilots
Association, International (ALPA), who supported the NPRM without
change.
The FAA received additional comments from five commenters,
including American Airlines (AAL), Delta Air Lines (DAL), FedEx Express
(FedEx), United Airlines (UAL), and an individual. The following
presents the comments received on the NPRM and the FAA's response to
each comment.
Request To Revise Applicability
AAL and UAL suggested revising the applicability statement to
include more aircraft manufacturers and models. AAL suggested adding
all airplane models that affected assemblies could be installed on, in
particular, Boeing Model 737-NG (Next Generation models are 737-600, -
700, -700C, -800, -900, and -900ER series), 737-MAX, 777-200, and 777-
300 series airplanes. UAL also suggested adding Model 737-NG airplanes.
AAL stated that the applicability statement as proposed in the NPRM
could mislead operators into believing that the AD would apply only to
the airplanes identified in paragraphs (c)(1) through (12) of the AD.
UAL believed the suggested change will be beneficial and assist
operators in determining if their fleets are affected.
[[Page 10959]]
The FAA disagrees with the commenters' request. The FAA does not
have a comprehensive list of all possible affected aircraft. To address
the incomplete list, paragraph (c) of this AD identifies specific
airplane models in paragraph (c) of this AD, but also notes that the
assemblies are ``not limited to.'' The FAA has not changed the AD in
this regard.
Request To Revise Compliance Time for Parts
AAL stated that the 60-day compliance time should apply only to
valve assemblies that are installed on the aircraft and not ones in
stock. AAL believes the unsafe condition only exists when an assembly
is installed on an airplane, and for those assemblies that are not
installed on an airplane, the proposed requirements in paragraph (k) of
the proposed AD would ensure that the unsafe condition is addressed
before that assembly is installed on an aircraft.
The FAA disagrees with the request to revise the compliance time.
The FAA agrees that an affected spare part that is uninstalled and
stored off an aircraft would not cause an unsafe condition on an
aircraft. The 60-day compliance time applies to parts already installed
on an aircraft, and paragraph (k) requires that action to be done on
affected spare parts before installation, which could result in a spare
part being inspected before the 60-day compliance time. In developing
the compliance time for this AD, the FAA considered the urgency
associated with the subject unsafe condition and the availability of
required parts. The FAA determined that the 60-day compliance time for
parts already installed on an aircraft is appropriate for accomplishing
the actions required by this AD while maintaining an adequate level of
safety. The FAA has not changed this AD in this regard.
Request To Remove Inspection for Serial Numbers or Include Only Valve
P/Ns
AAL requested that the inspection to verify the serial number of
the oxygen cylinder and entire assembly not be required. DAL requested
that paragraphs (c), (h), (i), and (k) of the proposed AD be revised to
remove reference to cylinder part numbers (P/Ns) and apply only to
valve assembly P/Ns. AAL stated that it reviewed the service
information and it seems that the defective part is only the valve
assembly or ``hand valve.'' DAL also reasoned that the unsafe condition
applies only to the valve assembly and not the cylinder. AAL then
reasoned that the inspection to verify the serial number should apply
only to the valve assembly or ``hand valve.'' AAL also stated that
paragraph (i) of the proposed AD also seems to require the actions of
paragraph (h)(1) through (3) of the proposed AD if a serial number of a
cylinder was affected and a valve assembly not affected, even though it
seems that it should not require those actions.
The FAA disagrees with the request. The parts of the oxygen
cylinder and valve assemblies are interrelated, and valves from matched
sets could have fit-up issues between parts or be mixed up or swapped
during maintenance operations. The serial number inspection as proposed
would address this interchangeability. The valve and cylinder that are
part of those assemblies must also be inspected to address the unsafe
condition, not just the assemblies themselves. Therefore, the FAA
specifies to inspect the oxygen valve assemblies, and oxygen cylinder
and valve assemblies, to determine the serial number of the valve,
cylinder, and entire assembly. The FAA has not changed this AD in this
regard.
Request To Clarify Which Components Need To Be Identified
UAL requested a change to the wording of which components need the
serial number inspection. UAL stated that the statement in paragraph
(h) of the proposed AD can be misconstrued as requiring that each of
the three components (valve, cylinder, and entire assembly) be
inspected individually for suspect serial numbers. UAL inferred that
the intention is to inspect for the serial number of the entire
cylinder and valve assembly, and not the individual components. UAL
also stated that, for new oxygen cylinder assemblies from AVOX, there
are individual placards that itemize the P/N and serial number for each
component, and that for some cylinder assemblies, the serialization of
the entire cylinder and valve assembly is nearly identical in format to
the serialization of sub-component valve assemblies, which could lead
to inaccurate reporting of results. The FAA infers that UAL suggested
that the relevant numbers on the placards could be confused with other
numbers.
The FAA disagrees. Each part and assembly stated in paragraph (h)
of this AD are interrelated and must be inspected. The valve and
cylinder components that are part of those assemblies must also be
inspected for serial numbers, not just the assemblies themselves. If
the serial number markings are unclear or missing, the service
information contains information on identifying the parts and part
assemblies. The FAA has not changed this AD in this regard.
Request To Revise Conditions for Gap Inspection and Related Actions
AAL and DAL requested changes to address concerns about what
actions are required if a part is missing a blue dot. DAL stated that
it seems best to prohibit all affected serial numbers to avoid a case
where an inspected and marked part is installed, but the blue dot
fades. AAL pointed to paragraph (i) of the proposed AD that would
clarify that only the affected serial numbers of the valve assembly
would need additional work, and, for valve assemblies marked with a
blue dot, a detailed inspection for correct spacing of the gap between
the bottom of the packing retainer and top of the valve body would not
be required. AAL stated that, as written, the proposed AD seems to
suggest that an inspection of the gap would be required regardless of
the presence of a blue dot.
The FAA disagrees with the request. The service information
specifies that if there is a doubt on the condition of a part, such as
missing serial numbers or a blue dot not definitively identified, then
the follow-on inspections are required to ensure that no discrepant or
affected part is missed. Paragraph (k) of this AD prohibits
installation of assemblies with affected serial numbers unless the
actions of paragraph (i) of this AD are accomplished. The FAA has not
changed this AD in this regard.
Request To Remove Inspection Report Requirement
DAL requested that the compliance times for the inspection report
be removed from paragraph (j)(1) of the proposed NPRM, and if not, the
inspection report itself be removed. AAL requested removing the
proposed requirement to submit an inspection report after accomplishing
the requirements (i.e., gap inspection) of paragraph (i) of the
proposed AD. FedEx stated reporting should not be required for units
that pass the inspection, and that sending units that failed the
inspection to the vendor should be sufficient for reporting those
failures. FedEx noted that any reporting requirements should consider
the difficulties in reporting findings in a short period of time and
noted that the inspector might not have access to the internet, email,
and a device capable of printing and scanning. FedEx opined that its
proposal would maintain accurate reporting and accommodate the
realities of a global workplace. AAL and DAL stated that the reporting
seems unnecessary and does not contribute to any additional level of
safety. AAL
[[Page 10960]]
added that the NPRM would give operators the responsibility of ensuring
that any affected part is returned to the manufacturer, and asserted
that an equivalent level of safety would be maintained even if the
reporting is not accomplished. DAL reasoned that if a cylinder valve
assembly is unacceptable, it would be in the operator's best interest
to report that finding to AVOX anyways so that it can receive a
replacement assembly.
The FAA disagrees. In this case, the inspection results need to be
reported to assist in tracking affected parts that are in circulation.
In addition, reporting all findings gives assurance that an inspection
was performed on an assembly with a given serial number. The FAA has
not changed this AD in this regard.
Request To Remove Compliance Time for Returning Parts
AAL, DAL, and UAL requested revising paragraph (j)(2) of the
proposed AD to remove a compliance time for returning discrepant parts
to the manufacturer. AAL stated that a compliance time would not
contribute to the level of safety. AAL also stated that all discrepant
assemblies would be returned in a timely manner that is sufficient to
the operator. DAL stated that it would be an unnecessary burden on
operators to wait for AVOX's response before sending an unacceptable or
discrepant part back within the compliance time in exchange for a free-
of-charge replacement. DAL also stated that it would also be in the
operator's best interest to send in the assembly so that it can qualify
for a free-of-charge replacement if AVOX determines the part is
unacceptable or discrepant. UAL stated it also believes the instruction
to contact AVOX for shipping instructions could impede compliance with
the 30-day limit to ship discrepant parts back to AVOX. UAL also stated
that it wants to know how, for accurate AD-compliance reporting, it
would be determined that a part is being shipped back as a result of
this finding from AD-required inspections, or as a result of other,
normal repair order processes.
The FAA agrees to clarify. Paragraph (j)(2) of this AD requires
returning the assembly to the manufacturer in accordance with paragraph
3.D.(2) or 3.D.(3), as applicable, of the applicable service
information. However, the service information does not include
instructions to wait for a response from AVOX before returning the
part. In addition, the FAA has revised paragraph (j)(2) of this AD to
clarify that contacting AVOX for shipping instructions in not required.
AVOX is tracking parts that are returned to it during accomplishment of
the AD for data collection or analysis of manufacturing issues, and
AVOX is also re-conditioning parts where possible. The FAA determined
that having a 30-day compliance time for returning the part after an
inspection finding is appropriate for this AD. However, under the
provisions of paragraph (m) of this AD, an operator may request an
approval of an alternative method of compliance (AMOC). The FAA has not
changed this AD in this regard.
Request To Allow Later Revisions of Service Information
AAL requested that all the references to the AVOX service
information be revised to allow use of subsequent revisions. AAL
reasoned that this revision would reduce the number of AMOC requests
each time a referenced service bulletin is revised.
The FAA disagrees. In an AD, the FAA may not refer to any document
that does not yet exist. In general terms, the FAA is required by the
Office of the Federal Register (OFR) regulations for approval of
materials incorporated by reference, as specified in 1 CFR 51.1(f), to
either publish the service document contents as part of the actual AD
language; or submit the service document to the OFR for approval as
referenced material, in which case the FAA may only refer to such
material in the text of an AD. The AD may refer to the service document
only if the OFR approved it for incorporation by reference. See 1 CFR
part 51. The FAA disagrees with revising the AD to include specific
airplane models based on the corresponding service information because
the agency does not have a comprehensive list of the applicable
aircraft to which specific AVOX service information could apply. The
FAA has not changed this AD in this regard.
Request To Clarify AD Applicability With Reference to Service
Information
A commenter requested clarifying paragraph (c) of the proposed AD
by including reference to the service information that was identified
in paragraph (h) of the proposed AD. The commenter suggested revising
the paragraph so that the applicability would include information on
the service information definition of the affected units. AAL also
requested adding the airplane configuration information in the text of
the AD to add further clarification to operators and release the
technical data in a more organized fashion.
The FAA disagrees. The definition of the affected units does not
need to be moved to paragraph (c) of the AD. The effectivity of the
service information is limited to specific airplane models, but the
applicability of this AD applies to all aircraft. Because the affected
parts could be installed on additional aircraft models, the FAA has
determined that the affected parts could later be installed on aircraft
that were initially delivered with acceptable parts, thereby subjecting
those aircraft to the unsafe condition. The FAA has not changed this AD
in this regard.
Request To Revise Compliance Time for Parts Identification
DAL and UAL requested revising the compliance time proposed in
paragraph (h) of the proposed NPRM. DAL and UAL stated that since many
operators have parked their aircraft or severely reduced usage of
aircraft, an extension of the compliance time (either with additional
calendar days or adding an option for flight hours and flight cycles),
would allow operators additional time for compliance. UAL also stated
that the supply chain could be affected due to potential increased
shipping time and workforce reductions.
The FAA disagrees with the request to extend the compliance time.
The FAA acknowledges the effects that the pandemic response might have
on operators' fleet use, supply chain, and maintenance personnel. In
developing an appropriate compliance time for this action, the FAA
considered the degree of urgency associated with addressing the subject
unsafe condition, the manufacturer's recommendation for an appropriate
compliance time, and the practical aspect of accomplishing the required
inspection within a period of time that corresponds to the normal
scheduled maintenance for most affected operators. In addition, the FAA
notes that some aircraft may have been in service during the pandemic
and must comply within the required compliance time. Operators do have
the option to inspect the airplane before the first flight following
storage if the airplane is in storage for more than 27 months. However,
under the provisions of paragraph (m) of this AD, the FAA will consider
requests for an extension of the compliance time if sufficient data are
submitted to substantiate that the new compliance time would provide an
acceptable level of safety. The FAA has not changed this AD in this
regard.
Request To Allow Use of Alternatives for Parts Marking
FedEx requested that the specification to use oil-based blue ink
markers be
[[Page 10961]]
modified to allow alternative methods and colors such as black
indelible ink. FedEx stated that oil-based blue paint markers are not
readily available or kept in stock regularly. FedEx suggested that a
list of part numbers for approved, aircraft grade, oil-based paint be
provided.
The FAA disagrees. While the FAA realizes this is a limitation,
there must be one standard to help avoid confusion. The procedures
required by this AD specify actions based on the presence or absence of
a blue dot in a specific location. The FAA has not seen any
difficulties in obtaining the paint markers. However, under the
provisions of paragraph (m) of this AD, any person may request an
approval of an AMOC. The FAA has not revised this AD in this regard.
Request To Allow Alternative Means of Measuring Gaps
FedEx requested that the proposed AD be revised to allow use of
feeler gauges, calipers, and other means of measuring the gap in
imperial units of measure. FedEx stated that the service information
specifies use of pin gauges that are made for metric units of measure,
and that acquiring those metric pin gauges is an extra expense and
logistical complication. FedEx recommended adding a tolerance to the
gap measurement and specifying a fractional imperial measure (\3/32\-
inch) that is close to the metric unit specified. FedEx suggested that
if a tolerance or other measurement is not added, then a manufacturer
part number (MPN) for a specific tool or supplier should be provided.
The FAA disagrees. Using other means of measuring could introduce
or increase variables that could affect the accuracy of the
measurement. The FAA understands that not everyone has the same
resources, tools, or supplies; however, the FAA also understands that
this means of measurement is easily accessible. Under the provisions of
paragraph (m) of this AD, operators may request approval of an AMOC if
sufficient data are submitted to substantiate that the tolerance would
provide an acceptable level of safety. The FAA has not changed this AD
in this regard.
Request To Revise Procedure for Shipping an Assembly
FedEx requested that the proposed AD be revised to allow operators
to use their own procedures for shipping dangerous goods such as
unopened cylinder valve assemblies (CVAs) instead of the procedure
specified in the service information. FedEx explained that it has
established and accepted procedures for shipping dangerous goods, and
that the disposition of an unopened CVA would be done by a department
separate from the one doing the inspection. FedEx stated that following
the procedures in the service information would require additional
coordination time, and that the wording of the procedures would not
function properly with its AD compliance mechanisms.
The FAA agrees to clarify. The design approval holder (DAH) of the
affected valve assemblies has specified a method for shipping, or
returning, an unopened CVA that has been found to be unacceptable or
discrepant, specifically a shipping method that is compliant with DOT
standard HM-224B. If FedEx has procedures that are compliant with DOT
standard HM-224B, then those procedures are acceptable for compliance
with this AD. For procedures that are not compliant with DOT standard
HM-224B, under the provisions of paragraph (m) of this AD, the FAA will
consider requests for an AMOC. The FAA has not changed this AD in this
regard.
Request for Clarification on Applicability of AD
FedEx requested clarification on whether the proposed AD is written
``against'' the MPN or the serial numbers within that MPN. FedEx
explained the effects on the operator's workload and also on the
operational impact of a unit's overhaul cycle in conjunction with a 60-
day compliance time and the scope of the applicability. FedEx added
that a 180-day compliance time would be more reasonable.
The FAA agrees to clarify. The applicability of this AD is written
against the MPN and specific serial numbers, in addition to manufacture
dates of the assemblies. The FAA disagrees to revise the compliance
time because the FAA has determined that requirement based on a risk
calculation. The FAA has not changed this AD in that regard.
Request To Clarify Requirement if Component Number(s) Cannot Be
Determined
UAL requested clarification on what actions are required in the
event the P/N or serial number information cannot be determined. UAL
stated that as a result of in-service activity, that information might
be illegible, unintentionally obliterated, or missing from the placard.
UAL added that under its normal practices, whenever a part or serial
number cannot be determined, the part is considered suspect, made
unserviceable, and removed from service. UAL stated that, when the P/N
of the entire cylinder and valve assembly can be determined but not the
serial number, and the date of manufacture is between January and
November 2018, it wants to still be able to establish conformity by
inspecting for the presence of the blue dot and accomplish the
applicable service information instruction if the blue dot is missing.
UAL also stated that depending on the FAA's response to this request,
it may apply for an AMOC.
The FAA agrees to clarify. The service information states to
inspect for the manufacturing date, serial number, and the presence of
a blue dot. The service information then states that if there is doubt
or a determination cannot be made (such as the numbers or dot is not
clearly identified), to proceed with the follow-on inspection for
proper gap spacing (this follow-on inspection is required by paragraph
(i) of this AD). The FAA has not changed this AD in this regard.
Request for Clarification on Compliance Time and Method for Inspection
Report
UAL requested clarification on how a 30-day requirement for the
inspection report was determined, and if a ``comprehensive'' report is
acceptable. UAL stated that it understands the need for the information
gathered from the reports; however, it does not understand why or how a
30-day compliance time was established. UAL also stated that it assumed
that reporting of the results should be done as a single, comprehensive
report and not piece-wise (individually for each assembly or aircraft),
and that the report does not need to be an exact copy of the report
form in the service information.
The FAA agrees to clarify. The FAA determined that the 30-day
compliance time is appropriate for this AD. Also, the manufacturer is
collecting information for analysis of manufacturing issues. The format
of the report may be done as UAL assumed, as long as all documents are
labeled correctly. However, under the provisions of paragraph (m) of
this AD, an operator may request an approval of an AMOC. The FAA has
not changed this AD in this regard.
Request To Provide Clarification on Reporting Form
UAL requested clarification on the definition of ``manufacture
date'' in a recording column of a report form in the service
information. UAL stated that it is implied that ``manufacture date'' in
that column is the manufacture date of
[[Page 10962]]
the entire cylinder and valve assembly and not of the valve assembly.
The FAA agrees to clarify. The ``manufacturer date'' is not limited
to the date of the entire cylinder and valve assembly, but is the
manufacture date of each part or assembly that might be recorded in the
inspection report, such as the assemblies listed in Appendix 1 of the
service information. The FAA has not changed this AD in this regard.
Conclusion
The FAA reviewed the relevant data, considered any comments
received, and determined that air safety requires adopting this AD as
proposed. Except for minor editorial changes, this AD is adopted as
proposed in the NPRM. None of the changes will increase the economic
burden on any operator.
Related Service Information Under 1 CFR Part 51
The FAA reviewed AVOX Systems Inc. Alert Service Bulletins
10015804-35-01, Revision 02, dated October 16, 2019; 10015804-35-02,
Revision 2, dated October 31, 2019; and 10015804-35-03, Revision 02,
dated October 15, 2019. This service information describes procedures
for an inspection to determine the serial numbers of the oxygen
cylinder and valve assemblies, and the oxygen valve assemblies, a
detailed inspection for correct spacing of the gap between the bottom
of the packing retainer and top of the valve body on the assemblies,
parts marking, inspection report, and return of parts to the
manufacturer. These documents are distinct since they apply to
different assembly part numbers. This service information is reasonably
available because the interested parties have access to it through
their normal course of business or by the means identified in
ADDRESSES.
Costs of Compliance
The FAA estimates that this AD affects up to 3,034 oxygen cylinder
and valve assemblies, and oxygen valve assemblies, installed on various
transport category airplanes of U.S. registry. The FAA estimates the
following costs to comply with this AD:
Estimated Costs
----------------------------------------------------------------------------------------------------------------
Cost per Cost on U.S.
Action Labor cost Parts cost product operators
----------------------------------------------------------------------------------------------------------------
Serial number inspection......... 1 work-hour x $85 None.................... $85 $257,890
per hour = $85.
Reporting........................ 1 work-hour x $85 0....................... 85 257,890
per hour = $85.
----------------------------------------------------------------------------------------------------------------
The FAA estimates the following costs to do any necessary follow-on
actions that would be required based on the results of the inspection.
The FAA has no way of determining the number of aircraft that might
need these actions:
On-Condition Costs *
----------------------------------------------------------------------------------------------------------------
Cost per
Action Labor cost Parts cost product
----------------------------------------------------------------------------------------------------------------
Detailed inspection................... 1 work-hour x $85 per None......................... $85
hour = $85.
----------------------------------------------------------------------------------------------------------------
* The FAA has received no definitive data on the cost of on-condition replacements.
According to the manufacturer, some or all of the costs of this AD
may be covered under warranty, thereby reducing the cost impact on
affected operators. The FAA does not control warranty coverage for
affected operators. As a result, the FAA has included all known costs
in the cost estimate.
Paperwork Reduction Act
A federal agency may not conduct or sponsor, and a person is not
required to respond to, nor shall a person be subject to a penalty for
failure to comply with a collection of information subject to the
requirements of the Paperwork Reduction Act unless that collection of
information displays a currently valid OMB Control Number. The OMB
Control Number for this information collection is 2120-0056. Public
reporting for this collection of information is estimated to take
approximately 1 hour per response, including the time for reviewing
instructions, searching existing data sources, gathering and
maintaining the data needed, and completing and reviewing the
collection of information. All responses to this collection of
information are mandatory. Send comments regarding this burden estimate
or any other aspect of this collection of information, including
suggestions for reducing this burden to: Information Collection
Clearance Officer, Federal Aviation Administration, 10101 Hillwood
Parkway, Fort Worth, TX 76177-1524.
Authority for This Rulemaking
Title 49 of the United States Code specifies the FAA's authority to
issue rules on aviation safety. Subtitle I, section 106, describes the
authority of the FAA Administrator. Subtitle VII: Aviation Programs,
describes in more detail the scope of the Agency's authority.
The FAA is issuing this rulemaking under the authority described in
Subtitle VII, Part A, Subpart III, Section 44701: General requirements.
Under that section, Congress charges the FAA with promoting safe flight
of civil aircraft in air commerce by prescribing regulations for
practices, methods, and procedures the Administrator finds necessary
for safety in air commerce. This regulation is within the scope of that
authority because it addresses an unsafe condition that is likely to
exist or develop on products identified in this rulemaking action.
Regulatory Findings
This AD will not have federalism implications under Executive Order
13132. This AD will not have a substantial direct effect on the States,
on the relationship between the national government and the States, or
on the distribution of power and responsibilities among the various
levels of government.
For the reasons discussed above, I certify that this AD:
(1) Is not a ``significant regulatory action'' under Executive
Order 12866,
(2) Will not affect intrastate aviation in Alaska, and
(3) Will not have a significant economic impact, positive or
negative, on a substantial number of small entities
[[Page 10963]]
under the criteria of the Regulatory Flexibility Act.
List of Subjects in 14 CFR Part 39
Air transportation, Aircraft, Aviation safety, Incorporation by
reference, Safety.
The Amendment
Accordingly, under the authority delegated to me by the
Administrator, the FAA amends 14 CFR part 39 as follows:
PART 39--AIRWORTHINESS DIRECTIVES
0
1. The authority citation for part 39 continues to read as follows:
Authority: 49 U.S.C. 106(g), 40113, 44701.
Sec. 39.13 [Amended]
0
2. The FAA amends Sec. 39.13 by adding the following new airworthiness
directive:
2022-04-09 AVOX Systems Inc. (formerly Scott Aviation): Amendment
39-21951; Docket No. FAA-2020-0345; Product Identifier 2019-NM-154-
AD.
(a) Effective Date
This airworthiness directive (AD) is effective April 4, 2022.
(b) Affected ADs
None.
(c) Applicability
This AD applies to AVOX Systems Inc. (formerly Scott Aviation)
oxygen cylinder and valve assemblies having part number (P/N)
89794077, 89794015, 891511-14, 806835-01, 807982-01, or 808433-01;
and oxygen valve assemblies (body and gage assemblies) having P/N
807206-01. These assemblies might be installed on, but not limited
to, the aircraft identified in paragraphs (c)(1) through (12) of
this AD, certificated in any category.
(1) Airbus SAS Model A300 B2-1A, B2-1C, B2K-3C, B2-203, B4-2C,
B4-103, and B4-203 airplanes.
(2) Airbus SAS Model A300 B4-601, B4-603, B4-620, B4-622, B4-
605R, B4-622R, F4-605R, F4-622R, and C4-605R Variant F airplanes.
(3) Airbus SAS Model A310-203, -204, -221, -222, -304, -322, -
324, and -325 airplanes.
(4) Airbus SAS Model A318-111, -112, -121, and -122 airplanes.
(5) Airbus SAS Model A319-111, -112, -113, -114, -115, -131, -
132, -133, and -151N airplanes.
(6) Airbus SAS Model A320-211, -212, -214, -216, -231, -232, -
233, -251N, -252N, -253N, -271N, -272N, and -273N airplanes.
(7) Airbus SAS Model A321-111, -112, -131, -211, -212, -213, -
231, -232, -251N, -252N, -253N, -271N, -272N, -251NX, -252NX, -
253NX, -271NX, and -272NX airplanes.
(8) Airbus SAS Model A330-201, -202, -203, -223, -243, -301, -
302, -303, -321, -322, -323, -341, -342, -343, and -941 airplanes.
(9) Airbus Model A340-211, -212, -213, -311, -312, -313, -541,
and -642 airplanes.
(10) ATR--GIE Avions de Transport R[eacute]gional Model ATR42-
200, -300, -320, and -500 airplanes.
(11) ATR--GIE Avions de Transport R[eacute]gional Model ATR72-
101, -102, -201, -202, -211, -212, and -212A airplanes.
(12) The Boeing Company Model 747-8 series airplanes.
(d) Subject
Air Transport Association (ATA) of America Code 35, Oxygen
System.
(e) Unsafe Condition
This AD was prompted by reports of cylinder and valve assemblies
having oxygen leakage from the valve assembly vent hole, caused by
the absence of a guide that maintains appropriate spacing between
certain parts. The FAA is issuing this AD to address oxygen leakage
from the cylinder, which could result in decreased or insufficient
oxygen supply during a depressurization event; and heating or flow
friction, which could cause an ignition event in the valve assembly.
(f) Compliance
Comply with this AD within the compliance times specified,
unless already done.
(g) Definition of Detailed Inspection
For the purposes of this AD, a detailed inspection is an
intensive examination of a specific item, installation, or assembly
to detect damage, failure, or irregularity. Available lighting is
normally supplemented with a direct source of good lighting at an
intensity deemed appropriate. Inspection aids such as mirror,
magnifying lenses, etc., may be necessary. Surface cleaning and
elaborate procedures may be required.
(h) Identification of Affected Cylinder and Valve Assemblies
Within 60 days after the effective date of this AD, inspect the
oxygen valve assemblies, and oxygen cylinder and valve assemblies,
to determine if the serial numbers of the valve, cylinder, and
entire assembly, are listed in Appendix 1, ``Affected Shipments,''
of the applicable service information identified in paragraphs
(h)(1) through (3) of this AD. A review of airplane maintenance
records is acceptable in lieu of this inspection if the serial
numbers can be conclusively determined from that review.
(1) AVOX Systems Inc. Alert Service Bulletin 10015804-35-01,
Revision 02, dated October 16, 2019.
(2) AVOX Systems Inc. Alert Service Bulletin 10015804-35-02,
Revision 2, dated October 31, 2019.
(3) AVOX Systems Inc. Alert Service Bulletin 10015804-35-03,
Revision 02, dated October 15, 2019.
(i) Inspection of the Gap, Parts Marking Actions, and Replacement
If, during any inspection or records review required by
paragraph (h) of this AD, any oxygen valve assembly, valve or
cylinder of an oxygen cylinder and valve assembly, or oxygen
cylinder and valve assembly having an affected serial number is
found: Before further flight, do a detailed inspection for correct
spacing of the gap between the bottom of the packing retainer and
top of the valve body, in accordance with paragraph 3.C. of the
Accomplishment Instructions of the applicable service information
identified in paragraphs (h)(1) through (3) of this AD.
(1) If the gap is found to be acceptable, as defined in the
applicable service information identified in paragraphs (h)(1)
through (3) of this AD, before further flight, do the parts marking
actions in accordance with paragraph 3.D.(1) of the Accomplishment
Instructions of the applicable service information identified in
paragraphs (h)(1) through (3) of this AD.
(2) If the gap is found to be unacceptable, as defined in the
applicable service information identified in paragraphs (h)(1)
through (3) of this AD, before further flight, remove the affected
assembly, in accordance with paragraphs 3.D.(2) or 3.D.(3), as
applicable, of the Accomplishment Instructions of the applicable
service information identified in paragraphs (h)(1) through (3) of
this AD; and replace with a serviceable assembly.
(j) Reporting and Return of Parts
(1) Report the results of the inspection required by paragraph
(i) of this AD within the applicable time specified in paragraph
(j)(1)(i) or (ii) of this AD. Report the results in accordance with
paragraph 3.D.(1)(a) of the Accomplishment Instructions of the
applicable service information identified in paragraphs (h)(1)
through (3) of this AD.
(i) If the inspection was done on or after the effective date of
this AD: Submit the report within 30 days after the inspection.
(ii) If the inspection was done before the effective date of
this AD: Submit the report within 30 days after the effective date
of this AD.
(2) If, during the inspection required by paragraph (i) of this
AD, any gap is found to be unacceptable, within the applicable time
specified in paragraph (j)(2)(i) or (ii) of this AD, return the
assembly to the manufacturer in accordance with paragraph 3.D.(2) or
3.D.(3), as applicable, of the Accomplishment Instructions of the
applicable service information identified in paragraphs (h)(1)
through (3) of this AD, except you are not required to contact AVOX
for shipping instructions.
(i) If the inspection was done on or after the effective date of
this AD: Return the assembly within 30 days after the inspection.
(ii) If the inspection was done before the effective date of
this AD: Return the assembly within 30 days after the effective date
of this AD.
(k) Parts Installation Limitation
As of the effective date of this AD, no AVOX Systems Inc. oxygen
valve assembly, or valve or cylinder that is part of an oxygen
cylinder and valve assembly, or oxygen cylinder and valve assembly
having an affected serial number identified in Appendix 1,
``Affected Shipments,'' of any AVOX Systems Inc. service information
[[Page 10964]]
identified in paragraphs (h)(1) through (3) of this AD may be
installed on any airplane unless the requirements of paragraph (i)
of this AD have been accomplished on that affected assembly.
(l) Credit for Previous Actions
This paragraph provides credit for the actions specified in
paragraphs (h) or (i) of this AD, if those actions were performed
before the effective date of this AD using the service information
specified in paragraphs (l)(1) through (5) of this AD.
(1) AVOX Systems Inc. Service Bulletin 10015804-35-01, dated
March 6, 2019.
(2) AVOX Systems Inc. Alert Service Bulletin 10015804-35-01,
Revision 01, dated July 9, 2019.
(3) AVOX Systems Inc. Alert Service Bulletin 10015804-35-02,
Revision 1, dated September 4, 2019.
(4) AVOX Systems Inc. Service Bulletin 10015804-35-03, dated
April 11, 2019.
(5) AVOX Systems Inc. Alert Service Bulletin 10015804-35-03,
Revision 01, dated May 21, 2019.
(m) Alternative Methods of Compliance (AMOCs)
(1) The Manager, New York ACO Branch, FAA, has the authority to
approve AMOCs for this AD, if requested using the procedures found
in 14 CFR 39.19. In accordance with 14 CFR 39.19, send your request
to your principal inspector or local Flight Standards District
Office, as appropriate. If sending information directly to the
manager of the certification office, send it to ATTN: Program
Manager, Continuing Operational Safety, FAA, New York ACO Branch,
1600 Stewart Avenue, Suite 410, Westbury, NY 11590; telephone 516-
228-7300; fax 516-794-5531.
(2) Before using any approved AMOC, notify your appropriate
principal inspector, or lacking a principal inspector, the manager
of the local flight standards district office/certificate holding
district office.
(n) Related Information
(1) For more information about this AD, contact Elizabeth
Dowling, Aerospace Engineer, Mechanical Systems and Administrative
Services Section, FAA, New York ACO Branch, 1600 Stewart Avenue,
Suite 410, Westbury, NY 11590; telephone 516-228-7300; email [email protected].
(2) Service information identified in this AD that is not
incorporated by reference is available at the addresses specified in
paragraphs (o)(3) and (4) of this AD.
(o) Material Incorporated by Reference
(1) The Director of the Federal Register approved the
incorporation by reference (IBR) of the service information listed
in this paragraph under 5 U.S.C. 552(a) and 1 CFR part 51.
(2) You must use this service information as applicable to do
the actions required by this AD, unless the AD specifies otherwise.
(i) AVOX Systems Inc. Alert Service Bulletin 10015804-35-01,
Revision 02, dated October 16, 2019.
(ii) AVOX Systems Inc. Alert Service Bulletin 10015804-35-02,
Revision 2, dated October 31, 2019.
(iii) AVOX Systems Inc. Alert Service Bulletin 10015804-35-03,
Revision 02, dated October 15, 2019.
(3) For service information identified in this AD, contact AVOX
Systems Inc., 225 Erie Street, Lancaster, NY 14086; telephone 716-
683-5100; internet https://www.safranaerosystems.com.
(4) You may view this service information at the FAA,
Airworthiness Products Section, Operational Safety Branch, 2200
South 216th St., Des Moines, WA. For information on the availability
of this material at the FAA, call 206-231-3195.
(5) You may view this service information that is incorporated
by reference at the National Archives and Records Administration
(NARA). For information on the availability of this material at
NARA, [email protected], or go to: https://www.archives.gov/federal-register/cfr/ibr-locations.html.
Issued on February 11, 2022.
Lance T. Gant,
Director, Compliance & Airworthiness Division, Aircraft Certification
Service.
[FR Doc. 2022-04146 Filed 2-25-22; 8:45 am]
BILLING CODE 4910-13-P