In the Matter of Certain Devices for Determining Organ Positions and Certain Subassemblies Thereof; Notice of Investigation, 72314-72315 [E5-6780]
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Federal Register / Vol. 70, No. 231 / Friday, December 2, 2005 / Notices
Fifth Principal Meridian, Minnesota
T. 141 N., R. 38 W.
The plat of survey represents the
dependent resurvey of a portion of the west
boundary, and a portion of the subdivisional
lines; and the survey of the subdivision of
section 18, Township 141 North, Range 38
West, of the Fifth Principal Meridian,
Minnesota, and was accepted November 23,
2005. We will place a copy of the plat we
described in the open files. It will be
available to the public as a matter of
information.
If BLM receives a protest against this
survey, as shown on the plat, prior to the
date of the official filing, we will stay the
filing pending our consideration of the
protest.
We will not officially file the plat until the
day after we have accepted or dismissed all
protests and they have become final,
including decisions on appeals.
Dated: November 23, 2005.
Jerry L. Wahl,
Chief Cadastral Surveyor.
[FR Doc. E5–6762 Filed 12–1–05; 8:45 am]
BILLING CODE 4310–GJ–P
DEPARTMENT OF THE INTERIOR
Bureau of Reclamation
Safety Modifications for Folsom Dam
and Appurtenant Structures (Folsom
Safety of Dams Project)—Sacramento,
El Dorado, and Placer Counties, CA
Bureau of Reclamation,
Interior.
ACTION: Notice of change to public
scoping meeting dates and locations.
AGENCY:
The notice of intent to
prepare an environmental impact
statement (EIS) and notice of public
scoping meetings was published in the
Federal Register on October 6, 2005 (70
FR 58469). The Bureau of Reclamation
is changing the public scoping meeting
dates from November 1 and 3, 2005, to
December 12 and 14, 2005. The scoping
meeting locations have also changed.
DATES: The new meeting dates are:
• December 12, 2005, 5 to 7 p.m.,
Granite Bay Activity Center, Folsom
State Recreation Area, CA.
• December 14, 2005, 5:30 to 8 p.m.,
Folsom, CA.
ADDRESSES: The new locations are:
• Granite Bay Activity Center, Folsom
State Recreation Area—there is no
address for this location. Directions
follow:
From Highway 50
(1) Take Hazel Avenue exit and head
north for 2 miles;
(2) Turn right on Madison Avenue
(becomes Greenback Lane at the car
15:11 Dec 01, 2005
Jkt 205001
From Interstate 80
(1) Take Douglas Boulevard exit and
head east for 6 miles;
(2) Go past the State Park’s entrance
station kiosk;
(3) Turn right at the 2nd stop sign;
and
(4) Turn left immediately (pass
through gate to Granite Bay Activity
Center).
• Folsom Community Center, 52
Natoma Street, Folsom, California.
FOR FURTHER INFORMATION CONTACT: Mr.
Shawn Oliver, Bureau of Reclamation,
7794 Folsom Dam Road, Folsom,
California 95630; telephone number
(916) 989–7256; e-mail
soliver@mp.usbr.gov.
Dated: November 17, 2005.
Frank Michny,
Regional Environmental Officer, Mid-Pacific
Region.
[FR Doc. E5–6757 Filed 12–1–05; 8:45 am]
BILLING CODE 4310–MN–P
SUMMARY:
VerDate Aug<31>2005
dealership) and head east a little over
2.5 miles;
(3) Turn left on Folsom-Auburn Road
and head north for 5 miles (if you go
over the bridge, you went too far);
(4) Turn right on Douglas Boulevard;
(5) Go past the State Park’s entrance
station kiosk;
(6) Turn right at the 2nd stop sign;
and
(7) Turn left immediately (pass
through gate to Granite Bay Activity
Center).
INTERNATIONAL TRADE
COMMISSION
[Investigation No. 337–TA–555]
In the Matter of Certain Devices for
Determining Organ Positions and
Certain Subassemblies Thereof; Notice
of Investigation
U.S. International Trade
Commission.
ACTION: Institution of investigation
pursuant to 19 U.S.C. 1337.
AGENCY:
SUMMARY: Notice is hereby given that a
complaint was filed with the U.S.
International Trade Commission on
September 28, 2005 under section 337
of the Tariff Act of 1930, as amended,
19 U.S.C. 1337, on behalf of SAS
PRAXIM of La Tronche, France and
Varian Medical Systems, Inc. of Palo
Alto, California. A supplement to the
complaint was filed on October 19,
2005. On October 25, 2005, the
Commission granted complainants’
request for a postponement of the
Commission’s determination whether to
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Sfmt 4703
institute an investigation in order for
complainant to provide further
supplementation. An additional
supplement was filed on November 9,
2005. The complaint, as supplemented,
alleges violations of section 337 in the
importation into the United States, the
sale for importation, and the sale within
the United States after importation of
certain devices for determining organ
positions and certain subassemblies
thereof by reason of infringement of
claims 1, 2, 5, and 10 of U.S. Patent No.
5,447,154. The complaint further alleges
that an industry in the United States
exists as required by subsection (a)(2) of
section 337.
The complainants request that the
Commission institute an investigation
and, after the investigation, issue a
permanent limited exclusion order and
a permanent cease and desist order.
ADDRESSES: The complaint and
supplements, except for any
confidential information contained
therein, are available for inspection
during official business hours (8:45 a.m.
to 5:15 p.m.) in the Office of the
Secretary, U.S. International Trade
Commission, 500 E Street, SW., Room
112, Washington, DC 20436, telephone
202–205–2000. Hearing-impaired
individuals are advised that information
on this matter can be obtained by
contacting the Commission’s TDD
terminal on 202–205–1810. Persons
with mobility impairments who will
need special assistance in gaining access
to the Commission should contact the
Office of the Secretary at 202–205–2000.
General information concerning the
Commission may also be obtained by
accessing its Internet server at https://
www.usitc.gov. The public record for
this investigation may be viewed on the
Commission’s electronic docket (EDIS)
at https://edis.usitc.gov.
FOR FURTHER INFORMATION CONTACT: Jay
H. Reiziss, Esq., Office of Unfair Import
Investigations, U.S. International Trade
Commission, telephone 202–205–2579.
Authority: The authority for institution of
this investigation is contained in section 337
of the Tariff Act of 1930, as amended, and
in § 210.10 of the Commission’s Rules of
Practice and Procedure, 19 CFR 210.10
(2005).
Scope of Investigation: Having
considered the complaint, the U.S.
International Trade Commission, on
November 23, 2005, Ordered that—
(1) Pursuant to subsection (b) of
section 337 of the Tariff Act of 1930, as
amended, an investigation be instituted
to determine whether there is a
violation of subsection (a)(1)(B) of
section 337 in the importation into the
United States, the sale for importation,
E:\FR\FM\02DEN1.SGM
02DEN1
Federal Register / Vol. 70, No. 231 / Friday, December 2, 2005 / Notices
or the sale within the United States after
importation of certain devices for
determining organ positions and certain
subassemblies thereof by reason of
infringement of claims 1, 2, 5, or 10 of
U.S. Patent No. 5,447,154, and whether
an industry in the United States exists
as required by subsection (a)(2) of
section 337.
(2) For the purpose of the
investigation so instituted, the following
are hereby named as parties upon which
this notice of investigation shall be
served:
(a) The complainants are—
SAS PRAXIM, 4 Avenue de l’Obiou,
Le Grand Sablon, 38700 La Tronche,
France.
Varian Medical Systems, Inc., 3100
Hansen Way, Palo Alto, California
94304.
(b) The respondent is the following
company alleged to be in violation of
section 337, and is the party upon
which the complaint is to be served:
Resonant Medical, Inc., 2050 Bleury
Street, Suite 200, Montreal, Quebec,
Canada H3A 2J5.
(c) Jay H. Reiziss, Esq., Office of
Unfair Import Investigations, U.S.
International Trade Commission, 500 E
Street, SW., Room 401–D, Washington,
DC 20436, who shall be the Commission
investigative attorney, party to this
investigation; and
(3) For the investigation so instituted,
the Honorable Charles E. Bullock is
designated as the presiding
administrative law judge.
A response to the complaint and the
notice of investigation must be
submitted by the named respondent in
accordance with § 210.13 of the
Commission’s Rules of Practice and
Procedure, 19 CFR 210.13. Pursuant to
19 CFR 201.16(d) and 210.13(a), such
response will be considered by the
Commission if received no later than 20
days after the date of service by the
Commission of the complaint and notice
of investigation. Extensions of time for
submitting a response to the complaint
will not be granted unless good cause
therefor is shown.
Failure of the respondent to file a
timely response to each allegation in the
complaint and in this notice may be
deemed to constitute a waiver of the
right to appear and contest the
allegations of the complaint and this
notice, and to authorize the
administrative law judge and the
Commission, without further notice to
the respondent, to find the facts to be as
alleged in the complaint and this notice
and to enter both an initial
determination and a final determination
containing such findings, and may
result in the issuance of a limited
VerDate Aug<31>2005
15:11 Dec 01, 2005
Jkt 205001
exclusion order or a cease and desist
order or both directed against such
respondent.
By order of the Commission.
Issued: November 28, 2005.
Marilyn R. Abbott,
Secretary to the Commission.
[FR Doc. E5–6780 Filed 12–1–05; 8:45 am]
BILLING CODE 7020–02–P
DEPARTMENT OF JUSTICE
[AAG/A Order No. 018–2005]
Privacy Act of 1974; Modification of
System of Records
Pursuant to the provisions of the
Privacy Act of 1974, 5 U.S.C. 552a,
notice is given that the Department of
Justice proposes to modify the
Departmentwide system of records
entitled, ‘‘Department of Justice
Regional Data Exchange System
(RDEX)’’ DOJ–012, previously published
in full text in the Federal Register on
July 11, 2005 (70 FR 39790).
This system is being modified as
follows:
(1) The Categories Of Individuals
Covered By The System And The
Categories Of Records In The System are
being modified to reflect that
information in RDEX that originated
with the Bureau of Alcohol, Tobacco,
Firearms, and Explosives (ATF), the
Drug Enforcement Administration
(DEA), and the Federal Bureau of
Investigation (FBI) will no longer be
limited to information from the State of
Washington field offices of those
components. This modification is
necessary due to the expansion of the
RDEX pilot project to include other
regional sharing initiatives;
(2) The Purpose Of the System is
being modified to reflect that in
addition to consolidating certain law
enforcement information from other
Department of Justice systems, in some
instances RDEX will include
information from such other systems
that has been structured in order to
facilitate sharing initiatives; and
(3) The System Managers and
Addresses portion of the notice is being
modified to reflect that requests for
information about the RDEX system
generally should be sent to the FBI
rather than the Chief Information
Officer, Justice Management Division, as
it was subsequently determined that the
FBI would serve as the system and
security administrator for RDEX.
The RDEX system is part of the
Department’s Law Enforcement
Information Sharing Program (LEISP).
The expansion of the RDEX pilot
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72315
program to include other regional
sharing initiatives and the concomitant
modifications to the RDEX system
notice to reflect such expansion serve to
further the LEISP’s principal purpose of
ensuring that Department of Justice
criminal law enforcement information is
available for users at all levels of
government so that they can more
effectively investigate, disrupt, and
deter criminal activity, including
terrorism, and protect the national
security.
The Department is providing a report
of this modification to OMB and
Congress.
Dated: November 22, 2005.
Paul R. Corts,
Assistant Attorney General for
Administration.
DOJ–012
SYSTEM NAME:
Department of Justice Regional Data
Exchange System (RDEX).
*
*
*
*
*
CATEGORIES OF INDIVIDUALS COVERED BY THE
SYSTEM:
Individuals covered by this system
include individuals who are referred to
in potential or actual cases or matters of
concern to the Federal Bureau of Prisons
(BOP), the United States Marshals
Service (USMS), the Bureau of Alcohol,
Tobacco, Firearms, and Explosives
(ATF), the Drug Enforcement
Administration (DEA), and the Federal
Bureau of Investigation (FBI). Because
the system contains audit logs regarding
queries, individuals who use the system
to conduct such queries are also
covered.
CATEGORIES OF RECORDS IN THE SYSTEM:
The system consists of unclassified
criminal law enforcement records
collected and produced by the BOP, the
USMS, the ATF, the DEA, and the FBI,
including: investigative reports and
witness interviews from both open and
closed cases; criminal event data (e.g.,
characteristics of criminal activities and
incidents that identify links or patterns);
criminal history information (e.g.,
history of arrests, nature and disposition
of criminal charges, sentencing,
confinement, and release); and
identifying information about criminal
offenders (e.g., name, address, date of
birth, birthplace, physical description).
The system also consists of audit logs
that contain information regarding
queries made of the system.
*
*
*
*
*
PURPOSE OF THE SYSTEM:
This system is maintained for the
purpose of ensuring that Department of
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02DEN1
Agencies
[Federal Register Volume 70, Number 231 (Friday, December 2, 2005)]
[Notices]
[Pages 72314-72315]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E5-6780]
=======================================================================
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INTERNATIONAL TRADE COMMISSION
[Investigation No. 337-TA-555]
In the Matter of Certain Devices for Determining Organ Positions
and Certain Subassemblies Thereof; Notice of Investigation
AGENCY: U.S. International Trade Commission.
ACTION: Institution of investigation pursuant to 19 U.S.C. 1337.
-----------------------------------------------------------------------
SUMMARY: Notice is hereby given that a complaint was filed with the
U.S. International Trade Commission on September 28, 2005 under section
337 of the Tariff Act of 1930, as amended, 19 U.S.C. 1337, on behalf of
SAS PRAXIM of La Tronche, France and Varian Medical Systems, Inc. of
Palo Alto, California. A supplement to the complaint was filed on
October 19, 2005. On October 25, 2005, the Commission granted
complainants' request for a postponement of the Commission's
determination whether to institute an investigation in order for
complainant to provide further supplementation. An additional
supplement was filed on November 9, 2005. The complaint, as
supplemented, alleges violations of section 337 in the importation into
the United States, the sale for importation, and the sale within the
United States after importation of certain devices for determining
organ positions and certain subassemblies thereof by reason of
infringement of claims 1, 2, 5, and 10 of U.S. Patent No. 5,447,154.
The complaint further alleges that an industry in the United States
exists as required by subsection (a)(2) of section 337.
The complainants request that the Commission institute an
investigation and, after the investigation, issue a permanent limited
exclusion order and a permanent cease and desist order.
ADDRESSES: The complaint and supplements, except for any confidential
information contained therein, are available for inspection during
official business hours (8:45 a.m. to 5:15 p.m.) in the Office of the
Secretary, U.S. International Trade Commission, 500 E Street, SW., Room
112, Washington, DC 20436, telephone 202-205-2000. Hearing-impaired
individuals are advised that information on this matter can be obtained
by contacting the Commission's TDD terminal on 202-205-1810. Persons
with mobility impairments who will need special assistance in gaining
access to the Commission should contact the Office of the Secretary at
202-205-2000. General information concerning the Commission may also be
obtained by accessing its Internet server at https://www.usitc.gov. The
public record for this investigation may be viewed on the Commission's
electronic docket (EDIS) at https://edis.usitc.gov.
FOR FURTHER INFORMATION CONTACT: Jay H. Reiziss, Esq., Office of Unfair
Import Investigations, U.S. International Trade Commission, telephone
202-205-2579.
Authority: The authority for institution of this investigation
is contained in section 337 of the Tariff Act of 1930, as amended,
and in Sec. 210.10 of the Commission's Rules of Practice and
Procedure, 19 CFR 210.10 (2005).
Scope of Investigation: Having considered the complaint, the U.S.
International Trade Commission, on November 23, 2005, Ordered that--
(1) Pursuant to subsection (b) of section 337 of the Tariff Act of
1930, as amended, an investigation be instituted to determine whether
there is a violation of subsection (a)(1)(B) of section 337 in the
importation into the United States, the sale for importation,
[[Page 72315]]
or the sale within the United States after importation of certain
devices for determining organ positions and certain subassemblies
thereof by reason of infringement of claims 1, 2, 5, or 10 of U.S.
Patent No. 5,447,154, and whether an industry in the United States
exists as required by subsection (a)(2) of section 337.
(2) For the purpose of the investigation so instituted, the
following are hereby named as parties upon which this notice of
investigation shall be served:
(a) The complainants are--
SAS PRAXIM, 4 Avenue de l'Obiou, Le Grand Sablon, 38700 La Tronche,
France.
Varian Medical Systems, Inc., 3100 Hansen Way, Palo Alto,
California 94304.
(b) The respondent is the following company alleged to be in
violation of section 337, and is the party upon which the complaint is
to be served:
Resonant Medical, Inc., 2050 Bleury Street, Suite 200, Montreal,
Quebec, Canada H3A 2J5.
(c) Jay H. Reiziss, Esq., Office of Unfair Import Investigations,
U.S. International Trade Commission, 500 E Street, SW., Room 401-D,
Washington, DC 20436, who shall be the Commission investigative
attorney, party to this investigation; and
(3) For the investigation so instituted, the Honorable Charles E.
Bullock is designated as the presiding administrative law judge.
A response to the complaint and the notice of investigation must be
submitted by the named respondent in accordance with Sec. 210.13 of
the Commission's Rules of Practice and Procedure, 19 CFR 210.13.
Pursuant to 19 CFR 201.16(d) and 210.13(a), such response will be
considered by the Commission if received no later than 20 days after
the date of service by the Commission of the complaint and notice of
investigation. Extensions of time for submitting a response to the
complaint will not be granted unless good cause therefor is shown.
Failure of the respondent to file a timely response to each
allegation in the complaint and in this notice may be deemed to
constitute a waiver of the right to appear and contest the allegations
of the complaint and this notice, and to authorize the administrative
law judge and the Commission, without further notice to the respondent,
to find the facts to be as alleged in the complaint and this notice and
to enter both an initial determination and a final determination
containing such findings, and may result in the issuance of a limited
exclusion order or a cease and desist order or both directed against
such respondent.
By order of the Commission.
Issued: November 28, 2005.
Marilyn R. Abbott,
Secretary to the Commission.
[FR Doc. E5-6780 Filed 12-1-05; 8:45 am]
BILLING CODE 7020-02-P