In the Matter of Certain Probe Card Assemblies, Components Thereof and Certain Tested DRAM and NAND Flash Memory Devices and Products Containing Same; Notice of Commission Determination To Review a Final Initial Determination in Part and Set a Schedule for Filing Written Submissions on the Issues Under Review and on Remedy, the Public Interest, and Bonding, 47822-47823 [E9-22381]
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Federal Register / Vol. 74, No. 179 / Thursday, September 17, 2009 / Notices
INTERNATIONAL TRADE
COMMISSION
[Investigation No. 337–TA–621]
In the Matter of Certain Probe Card
Assemblies, Components Thereof and
Certain Tested DRAM and NAND Flash
Memory Devices and Products
Containing Same; Notice of
Commission Determination To Review
a Final Initial Determination in Part and
Set a Schedule for Filing Written
Submissions on the Issues Under
Review and on Remedy, the Public
Interest, and Bonding
AGENCY: U.S. International Trade
Commission.
ACTION: Notice.
cprice-sewell on DSK2BSOYB1PROD with NOTICES
SUMMARY: Notice is hereby given that
the U.S. International Trade
Commission has determined to review
in part the final initial determination
(‘‘ID’’) issued by the presiding
administrative law judge (‘‘ALJ’’) on
June 29, 2009, in the above-captioned
investigation.
FOR FURTHER INFORMATION CONTACT:
Michael Liberman, Esq., Office of the
General Counsel, U.S. International
Trade Commission, 500 E Street, SW.,
Washington, DC 20436, telephone (202)
205–3116. Copies of non-confidential
documents filed in connection with this
investigation are or will be 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., Washington, DC 20436,
telephone (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. Hearing-impaired
persons are advised that information on
this matter can be obtained by
contacting the Commission’s TDD
terminal on (202) 205–1810.
SUPPLEMENTARY INFORMATION: This
investigation was instituted on
December 19, 2007, based on a
complaint filed by FormFactor, Inc.
(‘‘FormFactor’’) of Livermore, California.
The complaint alleged violations of
section 337 of the Tariff Act of 1930 (19
U.S.C. 1337) in the importation into the
United States, the sale for importation,
and the sale within the United States
after importation of certain probe card
assemblies, components thereof, and
certain tested DRAM and NAND flash
memory devices and products
containing same by reason of
VerDate Nov<24>2008
14:35 Sep 16, 2009
Jkt 217001
infringement of certain claims of U.S.
Patent Nos. 5,994,152; 6,509,751 (‘‘the
‘751 patent’’); 6,615,485; 6,624,648 (‘‘the
‘648’’patent); 7,168,162 (‘‘the ‘162
patent’’); and 7,225,538. The complaint
named Micronics Japan Co., Ltd.; MJC
Electronics Corp.; Phicom Corporation;
and Phiam Corporation as respondents
(collectively, ‘‘Respondents’’).
Subsequently, the ‘162 patent was
terminated from the investigation.
On December 5, 2008, respondents
Phicom Corp. and Phiam Corp.,
(collectively, ‘‘Phicom’’) jointly filed a
motion for partial summary
determination that claims 20 and 34 of
the ‘648 patent are invalid as indefinite
under 35 U.S.C. 112. On February 11,
2009, the ALJ issued an ID by Order No.
46. The subject ID states that ‘‘Phicom’s
motion * * * for summary
determination that the ‘648 patent is
invalid is * * * granted.’’ The ID
determines that claims 20 and 34, and
any asserted claims depending
therefrom, are invalid. Complainant
FormFactor filed a petition for review of
Order No. 46, which Respondents and
the Commission investigative attorney
oppose. On March 11, 2009, the
Commission determined to review
Order No. 46.
The evidentiary hearing in this
investigation was held from February
24, 2009 through March 6, 2009. On
June 29, 2009, the ALJ issued an Initial
Determination on Violation of Section
337 and Recommended Determination
on Remedy and Bond, finding no
violation of section 337. All parties to
this investigation, including the
Commission investigative attorney, filed
timely petitions for review of various
portions of the final ID, as well as timely
responses to the petitions.
Having examined the record in this
investigation, including the ALJ’s final
ID, the petitions for review, and the
responses thereto, the Commission has
determined to review the ID in part. In
particular, the Commission has
determined to review: (1) The ID’s
finding that Japanese Patent Application
Publication H10–31034 to Amamiya et
al. (‘‘Amamiya’’ or RX–166) does not
anticipate the asserted claims of the ‘751
patent under 35 U.S.C. 102; (2) the ID’s
conclusion of law regarding noninfringement of the ‘751 patent by
Phicom’s accused products; (3) the ID’s
conclusion that no analysis of the
validity of the asserted claims that
depend from claim 21 of the ‘152 patent
is needed. The Commission has
determined not to review the remainder
of the final ID.
On review, the Commission requests
the parties to brief their positions on the
issues under review with reference to
PO 00000
Frm 00046
Fmt 4703
Sfmt 4703
the applicable law and the evidentiary
record. The Commission is particularly
interested in responses to the following
questions:
(1) With respect to the ‘751 patent:
(a) What, if any, limitations are
missing from the Amamiya reference
such that it does not render the asserted
claims of the ‘751 patent invalid as
anticipated?
(b) Is there support for the
Commission investigative attorney’s and
Phicom’s argument that Amamiya
anticipates the asserted claims of the
‘751 patent, inter alia, by inherency? In
answering this question, address
paragraphs 0012 and 0013 on p. 6/8 of
Amamiya.
(c) Is the ID’s conclusion that there
has been no violation of section 337
with respect to the ‘751 patent
supported by its own findings?
(2) With respect to the ‘152 patent:
(a) Is the ID’s statement that ‘‘no
analysis of the invalidity arguments
related to anticipation and obviousness
of the dependent claims will be made,’’
ID at 191, consistent with the proper
analysis under patent law? If not, what,
if any, impact would such an error have
on the ID’s validity and infringement
analyses as to the ‘152 patent?
In connection with the final
disposition of this investigation, the
Commission may (1) issue an order that
could result in the exclusion of the
subject articles from entry into the
United States, and/or (2) issue one or
more cease and desist orders that could
result in the respondent being required
to cease and desist from engaging in
unfair acts in the importation and sale
of such articles. Accordingly, the
Commission is interested in receiving
written submissions that address the
form of remedy, if any, that should be
ordered. If a party seeks exclusion of an
article from entry into the United States
for purposes other than entry for
consumption, the party should so
indicate and provide information
establishing that activities involving
other types of entry either are adversely
affecting it or are likely to do so. For
background, see In the Matter of Certain
Devices for Connecting Computers via
Telephone Lines, Inv. No. 337–TA–360,
USITC Pub. No. 2843 (Dec. 1994)
(Commission Opinion).
If the Commission contemplates some
form of remedy, it must consider the
effects of that remedy upon the public
interest. The factors the Commission
will consider include the effect that an
exclusion order and/or cease and desist
orders would have on (1) The public
health and welfare, (2) competitive
conditions in the U.S. economy, (3) U.S.
E:\FR\FM\17SEN1.SGM
17SEN1
cprice-sewell on DSK2BSOYB1PROD with NOTICES
Federal Register / Vol. 74, No. 179 / Thursday, September 17, 2009 / Notices
production of articles that are like or
directly competitive with those that are
subject to investigation, and (4) U.S.
consumers. The Commission is
therefore interested in receiving written
submissions that address the
aforementioned public interest factors
in the context of this investigation.
If the Commission orders some form
of remedy, the U.S. Trade
Representative, as delegated by the
President, has 60 days to approve or
disapprove the Commission’s action.
See Presidential Memorandum of July
21, 2005. 70 FR 43251 (July 26, 2005).
During this period, the subject articles
would be entitled to enter the United
States under bond, in an amount
determined by the Commission. The
Commission is therefore interested in
receiving submissions concerning the
amount of the bond that should be
imposed.
Written Submissions: The parties to
the investigation are requested to file
written submissions on the issues under
review. The submissions should be
concise and thoroughly referenced to
the record in this investigation. Parties
to the investigation, interested
government agencies, and any other
interested parties are encouraged to file
written submissions on the issues of
remedy, the public interest, and
bonding. Such submissions should
address the recommended
determination by the ALJ on remedy
and bonding. Complainant and the
Commission investigative attorney are
also requested to submit proposed
remedial orders for the Commission’s
consideration. Complainant is further
requested to provide the expiration date
of the ‘751 patent and state the HTSUS
number under which the accused
articles are imported. The written
submissions and proposed remedial
orders must be filed no later than the
close of business on September 25,
2009. Reply submissions must be filed
no later than the close of business on
October 2, 2009. No further submissions
on these issues will be permitted unless
otherwise ordered by the Commission.
Persons filing written submissions
must file the original document and 12
true copies thereof on or before the
deadlines stated above with the Office
of the Secretary. Any person desiring to
submit a document (or portion thereof)
to the Commission in confidence must
request confidential treatment unless
the information has already been
granted such treatment during the
proceedings. All such requests should
be directed to the Secretary of the
Commission and must include a full
statement of the reasons why the
Commission should grant such
VerDate Nov<24>2008
14:35 Sep 16, 2009
Jkt 217001
treatment. See section 201.6 of the
Commission’s Rules of Practice and
Procedure, 19 CFR 201.6. Documents for
which confidential treatment by the
Commission is sought will be treated
accordingly. All nonconfidential written
submissions will be available for public
inspection at the Office of the Secretary.
The authority for the Commission’s
determination is contained in section
337 of the Tariff Act of 1930, as
amended (19 U.S.C. 1337), and in
sections 210.42–.46 of the Commission’s
Rules of Practice and Procedure (19 CFR
210.42–.46).
By order of the Commission.
Marilyn R. Abbott,
Secretary to the Commission.
Issued: September 14, 2009.
William R. Bishop,
Acting Secretary to the Commission.
[FR Doc. E9–22381 Filed 9–16–09; 8:45 am]
BILLING CODE P
DEPARTMENT OF JUSTICE
Notice of Lodging of Consent Decree
Under Comprehensive Environmental
Response, Compensation and Liability
Act
Notice is hereby given that on
September 10, 2009, a proposed Consent
Judgment in United States v. Genesco
Inc. No. CV–09–3917, was lodged with
the United States District Court for the
Eastern District of New York.
The proposed Consent Judgment
resolves certain claims of the United
States, on behalf of the Environmental
Protection Agency (‘‘EPA’’), under the
Comprehensive Environmental
Response, Compensation, and Liability
Act (‘‘CERCLA’’), 42 U.S.C. 9601 et seq.,
in connection with the Fulton Avenue
Superfund Site located in and around
the Village of Garden City Park in
Nassau County, New York (‘‘Site’’),
against defendant Genesco Inc.
(‘‘Genesco’’). The proposed Consent
Judgment requires Genesco to
implement the interim groundwater
extraction and treatment remedy
contained in EPA’s September 28, 2007
First Operable Unit (‘‘OU1’’) Record of
Decision (‘‘ROD’’) for the Site.
The proposed Consent Judgment
provides that Genesco is entitled to
contribution protection as provided by
section 113(f)(2) of CERCLA, 42 U.S.C.
9613(f)(2) for matters addressed by the
settlement.
The Department of Justice will receive
for a period of 30 days from the date of
this publication comments relating to
the proposed Consent Judgment.
Comments should be addressed to the
PO 00000
Frm 00047
Fmt 4703
Sfmt 4703
47823
Assistant Attorney General,
Environment and Natural Resources
Division, and either e-mailed to
pubcomment-ees.enrd@usdoj.gov or
mailed to P.O. Box 7611, U.S.
Department of Justice, Washington, DC
20044–7611, and should refer to: United
States v. Genesco Inc., No. CV–09–3917,
DOJ Ref. No. 90–11–2–09329.
The proposed Consent Judgment may
be examined at the Office of the United
States Attorney, Eastern District of New
York, 610 Federal Plaza, Central Islip,
New York 11722–4454. During the
public comment period, the proposed
Consent Judgment may also be
examined on the following Department
of Justice Web site, https://
www.usdoj.gov/enrd/
Consent_Decrees.html. A copy of the
proposed Consent Judgment may also be
obtained by mail from the Consent
Decree Library, P.O. Box 7611, U.S.
Department of Justice, Washington, DC
20044–7611 or by faxing or e-mailing a
request to Tonia Fleetwood
(tonia.fleetwood@usdoj.gov), fax no.
(202) 514–0097, phone confirmation
number (202) 514–1547. In requesting a
copy from the Consent Decree Library,
please enclose a check in the amount of
$46.50 (25 cents per page reproduction
cost), payable to the U.S. Treasury.
Maureen Katz,
Assistant Chief, Environmental Enforcement
Section, Environment and Natural Resources
Division.
[FR Doc. E9–22350 Filed 9–16–09; 8:45 am]
BILLING CODE 4410–15–P
DEPARTMENT OF JUSTICE
Antitrust Division
Notice Pursuant to the National
Cooperative Research and Production
Act of 1993—Pistoia Alliance, Inc.
Notice is hereby given that, on August
19, 2009, pursuant to section 6(a) of the
National Cooperative Research and
Production Act of 1993, 15 U.S.C.
§ 4301 et seq. (‘‘the Act’’), Pistoia
Alliance, Inc. has filed written
notifications simultaneously with the
Attorney General and the Federal Trade
Commission disclosing changes in its
membership. The notifications were
filed for the purpose of extending the
Act’s provisions limiting the recovery of
antitrust plaintiffs to actual damages
under specified circumstances.
Specifically, H. Lundbeck A/S, Valby,
Denmark; UPCO, Woking, United
Kingdom; Rescentris, Columbus, OH; F.
Hoffmann-La Roche LTD, Basel,
Switzerland; Bristol-Myers Squibb,
Princeton, NJ; KNIME.com GmbH,
E:\FR\FM\17SEN1.SGM
17SEN1
Agencies
[Federal Register Volume 74, Number 179 (Thursday, September 17, 2009)]
[Notices]
[Pages 47822-47823]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-22381]
[[Page 47822]]
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INTERNATIONAL TRADE COMMISSION
[Investigation No. 337-TA-621]
In the Matter of Certain Probe Card Assemblies, Components
Thereof and Certain Tested DRAM and NAND Flash Memory Devices and
Products Containing Same; Notice of Commission Determination To Review
a Final Initial Determination in Part and Set a Schedule for Filing
Written Submissions on the Issues Under Review and on Remedy, the
Public Interest, and Bonding
AGENCY: U.S. International Trade Commission.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: Notice is hereby given that the U.S. International Trade
Commission has determined to review in part the final initial
determination (``ID'') issued by the presiding administrative law judge
(``ALJ'') on June 29, 2009, in the above-captioned investigation.
FOR FURTHER INFORMATION CONTACT: Michael Liberman, Esq., Office of the
General Counsel, U.S. International Trade Commission, 500 E Street,
SW., Washington, DC 20436, telephone (202) 205-3116. Copies of non-
confidential documents filed in connection with this investigation are
or will be 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., Washington, DC
20436, telephone (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. Hearing-impaired persons are advised that information
on this matter can be obtained by contacting the Commission's TDD
terminal on (202) 205-1810.
SUPPLEMENTARY INFORMATION: This investigation was instituted on
December 19, 2007, based on a complaint filed by FormFactor, Inc.
(``FormFactor'') of Livermore, California. The complaint alleged
violations of section 337 of the Tariff Act of 1930 (19 U.S.C. 1337) in
the importation into the United States, the sale for importation, and
the sale within the United States after importation of certain probe
card assemblies, components thereof, and certain tested DRAM and NAND
flash memory devices and products containing same by reason of
infringement of certain claims of U.S. Patent Nos. 5,994,152; 6,509,751
(``the `751 patent''); 6,615,485; 6,624,648 (``the `648''patent);
7,168,162 (``the `162 patent''); and 7,225,538. The complaint named
Micronics Japan Co., Ltd.; MJC Electronics Corp.; Phicom Corporation;
and Phiam Corporation as respondents (collectively, ``Respondents'').
Subsequently, the `162 patent was terminated from the investigation.
On December 5, 2008, respondents Phicom Corp. and Phiam Corp.,
(collectively, ``Phicom'') jointly filed a motion for partial summary
determination that claims 20 and 34 of the `648 patent are invalid as
indefinite under 35 U.S.C. 112. On February 11, 2009, the ALJ issued an
ID by Order No. 46. The subject ID states that ``Phicom's motion * * *
for summary determination that the `648 patent is invalid is * * *
granted.'' The ID determines that claims 20 and 34, and any asserted
claims depending therefrom, are invalid. Complainant FormFactor filed a
petition for review of Order No. 46, which Respondents and the
Commission investigative attorney oppose. On March 11, 2009, the
Commission determined to review Order No. 46.
The evidentiary hearing in this investigation was held from
February 24, 2009 through March 6, 2009. On June 29, 2009, the ALJ
issued an Initial Determination on Violation of Section 337 and
Recommended Determination on Remedy and Bond, finding no violation of
section 337. All parties to this investigation, including the
Commission investigative attorney, filed timely petitions for review of
various portions of the final ID, as well as timely responses to the
petitions.
Having examined the record in this investigation, including the
ALJ's final ID, the petitions for review, and the responses thereto,
the Commission has determined to review the ID in part. In particular,
the Commission has determined to review: (1) The ID's finding that
Japanese Patent Application Publication H10-31034 to Amamiya et al.
(``Amamiya'' or RX-166) does not anticipate the asserted claims of the
`751 patent under 35 U.S.C. 102; (2) the ID's conclusion of law
regarding non-infringement of the `751 patent by Phicom's accused
products; (3) the ID's conclusion that no analysis of the validity of
the asserted claims that depend from claim 21 of the `152 patent is
needed. The Commission has determined not to review the remainder of
the final ID.
On review, the Commission requests the parties to brief their
positions on the issues under review with reference to the applicable
law and the evidentiary record. The Commission is particularly
interested in responses to the following questions:
(1) With respect to the `751 patent:
(a) What, if any, limitations are missing from the Amamiya
reference such that it does not render the asserted claims of the `751
patent invalid as anticipated?
(b) Is there support for the Commission investigative attorney's
and Phicom's argument that Amamiya anticipates the asserted claims of
the `751 patent, inter alia, by inherency? In answering this question,
address paragraphs 0012 and 0013 on p. 6/8 of Amamiya.
(c) Is the ID's conclusion that there has been no violation of
section 337 with respect to the `751 patent supported by its own
findings?
(2) With respect to the `152 patent:
(a) Is the ID's statement that ``no analysis of the invalidity
arguments related to anticipation and obviousness of the dependent
claims will be made,'' ID at 191, consistent with the proper analysis
under patent law? If not, what, if any, impact would such an error have
on the ID's validity and infringement analyses as to the `152 patent?
In connection with the final disposition of this investigation, the
Commission may (1) issue an order that could result in the exclusion of
the subject articles from entry into the United States, and/or (2)
issue one or more cease and desist orders that could result in the
respondent being required to cease and desist from engaging in unfair
acts in the importation and sale of such articles. Accordingly, the
Commission is interested in receiving written submissions that address
the form of remedy, if any, that should be ordered. If a party seeks
exclusion of an article from entry into the United States for purposes
other than entry for consumption, the party should so indicate and
provide information establishing that activities involving other types
of entry either are adversely affecting it or are likely to do so. For
background, see In the Matter of Certain Devices for Connecting
Computers via Telephone Lines, Inv. No. 337-TA-360, USITC Pub. No. 2843
(Dec. 1994) (Commission Opinion).
If the Commission contemplates some form of remedy, it must
consider the effects of that remedy upon the public interest. The
factors the Commission will consider include the effect that an
exclusion order and/or cease and desist orders would have on (1) The
public health and welfare, (2) competitive conditions in the U.S.
economy, (3) U.S.
[[Page 47823]]
production of articles that are like or directly competitive with those
that are subject to investigation, and (4) U.S. consumers. The
Commission is therefore interested in receiving written submissions
that address the aforementioned public interest factors in the context
of this investigation.
If the Commission orders some form of remedy, the U.S. Trade
Representative, as delegated by the President, has 60 days to approve
or disapprove the Commission's action. See Presidential Memorandum of
July 21, 2005. 70 FR 43251 (July 26, 2005). During this period, the
subject articles would be entitled to enter the United States under
bond, in an amount determined by the Commission. The Commission is
therefore interested in receiving submissions concerning the amount of
the bond that should be imposed.
Written Submissions: The parties to the investigation are requested
to file written submissions on the issues under review. The submissions
should be concise and thoroughly referenced to the record in this
investigation. Parties to the investigation, interested government
agencies, and any other interested parties are encouraged to file
written submissions on the issues of remedy, the public interest, and
bonding. Such submissions should address the recommended determination
by the ALJ on remedy and bonding. Complainant and the Commission
investigative attorney are also requested to submit proposed remedial
orders for the Commission's consideration. Complainant is further
requested to provide the expiration date of the `751 patent and state
the HTSUS number under which the accused articles are imported. The
written submissions and proposed remedial orders must be filed no later
than the close of business on September 25, 2009. Reply submissions
must be filed no later than the close of business on October 2, 2009.
No further submissions on these issues will be permitted unless
otherwise ordered by the Commission.
Persons filing written submissions must file the original document
and 12 true copies thereof on or before the deadlines stated above with
the Office of the Secretary. Any person desiring to submit a document
(or portion thereof) to the Commission in confidence must request
confidential treatment unless the information has already been granted
such treatment during the proceedings. All such requests should be
directed to the Secretary of the Commission and must include a full
statement of the reasons why the Commission should grant such
treatment. See section 201.6 of the Commission's Rules of Practice and
Procedure, 19 CFR 201.6. Documents for which confidential treatment by
the Commission is sought will be treated accordingly. All
nonconfidential written submissions will be available for public
inspection at the Office of the Secretary.
The authority for the Commission's determination is contained in
section 337 of the Tariff Act of 1930, as amended (19 U.S.C. 1337), and
in sections 210.42-.46 of the Commission's Rules of Practice and
Procedure (19 CFR 210.42-.46).
By order of the Commission.
Marilyn R. Abbott,
Secretary to the Commission.
Issued: September 14, 2009.
William R. Bishop,
Acting Secretary to the Commission.
[FR Doc. E9-22381 Filed 9-16-09; 8:45 am]
BILLING CODE P