Certain Taurine (2-Aminoethanesulfonic Acid), Methods of Production and Processes for Making the Same, and Products Containing the Same; Institution of Investigation, 8110-8112 [2019-03988]

Download as PDF 8110 Federal Register / Vol. 84, No. 44 / Wednesday, March 6, 2019 / Notices complaint alleges 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 data transmission devices, components thereof, associated software, and products containing the same. The complaint names as respondents: Apple Inc. of Cupertino, CA; Amazon.com, Inc. of Seattle, WA; Amazon Digital Services, LLC of Seattle, WA; Verizon Communications Inc. of New York, NY and Cellco Partnership d/b/a Verizon Wireless of Basking Ridge, NJ. The complainant requests that the Commission issue a limited exclusion order and cease and desist orders. Proposed respondents, other interested parties, and members of the public are invited to file comments, not to exceed five (5) pages in length, inclusive of attachments, on any public interest issues raised by the complaint or § 210.8(b) filing. Comments should address whether issuance of the relief specifically requested by the complainant in this investigation would affect the public health and welfare in the United States, competitive conditions in the United States economy, the production of like or directly competitive articles in the United States, or United States consumers. In particular, the Commission is interested in comments that: (i) Explain how the articles potentially subject to the requested remedial orders are used in the United States; (ii) identify any public health, safety, or welfare concerns in the United States relating to the requested remedial orders; (iii) identify like or directly competitive articles that complainant, its licensees, or third parties make in the United States which could replace the subject articles if they were to be excluded; (iv) indicate whether complainant, complainant’s licensees, and/or third party suppliers have the capacity to replace the volume of articles potentially subject to the requested exclusion order and/or a cease and desist order within a commercially reasonable time; and (v) explain how the requested remedial orders would impact United States consumers. Written submissions on the public interest must be filed no later than by close of business, eight calendar days after the date of publication of this notice in the Federal Register. There will be further opportunities for VerDate Sep<11>2014 18:35 Mar 05, 2019 Jkt 247001 comment on the public interest after the issuance of any final initial determination in this investigation. Any written submissions on other issues should be filed no later than by close of business nine calendar days after the date of publication of this notice in the Federal Register. Complainant may file a reply to any written submission no later than the date on which complainant’s reply would be due under § 210.8(c)(2) of the Commission’s Rules of Practice and Procedure (19 CFR 210.8(c)(2)). Persons filing written submissions must file the original document electronically on or before the deadlines stated above and submit 8 true paper copies to the Office of the Secretary by noon the next day pursuant to § 210.4(f) of the Commission’s Rules of Practice and Procedure (19 CFR 210.4(f)). Submissions should refer to the docket number (‘‘Docket No. 3368) in a prominent place on the cover page and/ or the first page. (See Handbook for Electronic Filing Procedures, Electronic Filing Procedures 1). Persons with questions regarding filing should contact the Secretary (202–205–2000). Any person desiring to submit a document to the Commission in confidence must request confidential treatment. All such requests should be directed to the Secretary to the Commission and must include a full statement of the reasons why the Commission should grant such treatment. See 19 CFR 201.6. Documents for which confidential treatment by the Commission is properly sought will be treated accordingly. All information, including confidential business information and documents for which confidential treatment is properly sought, submitted to the Commission for purposes of this Investigation may be disclosed to and used: (i) By the Commission, its employees and Offices, and contract personnel (a) for developing or maintaining the records of this or a related proceeding, or (b) in internal investigations, audits, reviews, and evaluations relating to the programs, personnel, and operations of the Commission including under 5 U.S.C. Appendix 3; or (ii) by U.S. government employees and contract personnel,2 solely for cybersecurity purposes. All nonconfidential written submissions will be available for public 1 Handbook for Electronic Filing Procedures: https://www.usitc.gov/documents/handbook_on_ filing_procedures.pdf. 2 All contract personnel will sign appropriate nondisclosure agreements. PO 00000 Frm 00040 Fmt 4703 Sfmt 4703 inspection at the Office of the Secretary and on EDIS.3 This action is taken under the authority of section 337 of the Tariff Act of 1930, as amended (19 U.S.C. 1337), and of §§ 201.10 and 210.8(c) of the Commission’s Rules of Practice and Procedure (19 CFR 201.10, 210.8(c)). By order of the Commission. Issued: March 1, 2019. Lisa Barton, Secretary to the Commission. [FR Doc. 2019–04039 Filed 3–5–19; 8:45 am] BILLING CODE 7020–02–P INTERNATIONAL TRADE COMMISSION [Investigation No. 337–TA–1146] Certain Taurine (2Aminoethanesulfonic Acid), Methods of Production and Processes for Making the Same, and Products Containing the Same; Institution of Investigation U.S. International Trade Commission. ACTION: Notice. AGENCY: Notice is hereby given that a complaint was filed with the U.S. International Trade Commission on January 30, 2019, under section 337 of the Tariff Act of 1930, as amended, on behalf of Vitaworks IP, LLC of North Brunswick, New Jersey; Vitaworks, LLC of North Brunswick, New Jersey; and Dr. Songzhou Hu of North Brunswick, New Jersey. Supplemental exhibits were filed February 19, 2019. The complaint alleges violations of section 337 based upon the importation into the United States, the sale for importation, and the sale within the United States after importation of certain taurine (2aminoethanesulfonic acid), methods of production and processes for making the same, and products containing the same by reason of infringement of certain claims of U.S. Patent No. 9,573,890 (‘‘the ’890 patent’’); U.S. Patent No. 9,745,258 (‘‘the ’258 patent’’); and U.S. Patent No. 10,040,755 (‘‘the ’755 patent’’). The complaint further alleges that an industry in the United States exists as required by the applicable Federal Statute. The complainants request that the Commission institute an investigation and, after the investigation, issue a limited exclusion order and cease and desist orders. ADDRESSES: The complaint, except for any confidential information contained SUMMARY: 3 Electronic Document Information System (EDIS): https://edis.usitc.gov. E:\FR\FM\06MRN1.SGM 06MRN1 Federal Register / Vol. 84, No. 44 / Wednesday, March 6, 2019 / Notices therein, is 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: Pathenia M. Proctor, The Office of Unfair Import Investigations, U.S. International Trade Commission, telephone (202) 205–2560. SUPPLEMENTARY INFORMATION: Authority: The authority for institution of this investigation is contained in section 337 of the Tariff Act of 1930, as amended, 19 U.S.C. 1337, and in section 210.10 of the Commission’s Rules of Practice and Procedure, 19 CFR 210.10 (2018). Scope of Investigation: Having considered the complaint, the U.S. International Trade Commission, on February 28, 2019, 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, or the sale within the United States after importation of certain products identified in paragraph (2) by reason of infringement of one or more of claims 1 and 3–10 of the ’890 patent; claims 1– 3 of the ’258 patent; and claims 1–9 of the ’755 patent; and whether an industry in the United States exists as required by subsection (a)(2) of section 337; (2) Pursuant to section 210.10(b)(1) of the Commission’s Rules of Practice and Procedure, 19 CFR 210.10(b)(1), the plain language description of the accused products or category of accused products, which defines the scope of the investigation, is ‘‘taurine in its raw form, or combined with chemical additives such as an anti-caking agent, manufactured through processes featuring the use of alkali isethionate or ammonium isethionate’’; VerDate Sep<11>2014 18:35 Mar 05, 2019 Jkt 247001 (3) Pursuant to section 210.10(b)(3) of the Commission’s Rules of Practice and Procedure, 19 CFR 210.10(b)(3), the presiding Administrative Law Judge shall hold an early evidentiary hearing, find facts, and issue an early decision, within 100 days of institution except for good cause shown, as to whether the complainants have satisfied the economic prong of the domestic industry requirement. Notwithstanding any Commission Rules to the contrary, which are hereby waived, any such decision should be issued in the form of an initial determination (ID) under Commission Rule 210.42(a)(3), 19 CFR 210.42(a)(3). The ID will become the Commission’s final determination 30 days after the date of service of the ID unless the Commission determines to review the ID. Any such review will be conducted in accordance with Commission Rules 210.43, 210.44, and 210.45, 19 CFR 210.43, 210.44, and 210.45. The issuance of an early ID finding that complainant does not satisfy the economic prong of the domestic industry requirement shall stay the investigation unless the Commission orders otherwise; any other decision shall not stay the investigation or delay the issuance of a final ID covering the other issues of the investigation; (4) 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: Vitaworks IP, LLC, 195 Black Horse Lane, North Brunswick, NJ 08902 Vitaworks, LLC, 195 Black Horse Lane, North Brunswick, NJ 08902 Dr. Songzhou Hu, 195 Black Horse Lane, North Brunswick, NJ 08902 (b) The respondents are the following entities alleged to be in violation of section 337, and are the parties upon which the complaint is to be served: A to Z Nutrition, Inc., 14359 Miramar Parkway, Suite 218, Miramar, FL 33027 Ampak Company, Inc., 1890 Palmer Avenue, Suite 301, Larchmont, NY 10538 Armada Nutrition LLC, 4637 Port Royal Road, Spring Hill, TN 37174 Atlantic Chemicals Trading of North America, Inc., 2 Oliver Street, Suite 602, Boston, MA 02109 Crossroad Ingredients LLC, 271 U.S. 46 West, Suite H206, Fairfield, NJ 07004 Emote International, Inc., 1736 Wright Avenue, La Verne, CA 91750 Epikix, Inc., 6 Imperial Aisle, Irvine, CA 92606 Fuerst Day Lawson (USA), Ltd., Metropolitan Wharf, 70 Wapping PO 00000 Frm 00041 Fmt 4703 Sfmt 4703 8111 Wall, London, England E1W 3SS, United Kingdom Glanbia Nurtitional (NA), Inc., 2840 Loker Avenue East, Carlsbad, CA 92101 Greating Shipping Co., 2225 W. Commonwealth Avenue, Suite 316, Alhambra, CA 91803 Green Wave Ingredients, Inc., 14821 Northam Street, La Mirada, CA 90638 Hard Eight Nutrition, LLC, 7511 Eastgate Road, Henderson, NV 89011 Fuchi Pharmaceutical Co., Ltd. d/b/a, Hubei Grand Life Science and Technology Co., Ltd., 12 Wangfen Road, Fuchi Town, Yangxin County, Hubei Province, China 435200 Jiangyin Huachang Food Additive Co., Ltd., No. 152, Yingbin West Road, Huangtu Town, JiangYin City, Jiang Su Province, China 214445 Natural Ingredient Corp., 155 N. Lake Avenue, 8th Floor, Suite 808, Pasadena, CA 91101 JSW Enterprises, LLC d/b/a, Nurtavative Ingredients, 600 Century Parkway, Suite 200, Allen, TX 75013 N.V.E., Inc. a/k/a, N.V.E. Pharmaceuticals, Inc., 15 Whitehall Road, Andover, NJ 07821 Pacific Rainbow International, Inc., 19905 Harrison Avenue, City of Industry, CA 91789 Pharmachem Laboratories, Inc., 265 Harrison Avenue, Kearny, NJ 07032 Prinova USA, LLC, 285 E. Fullerton Avenue, Carol Stream, IL 60188 Qianjiang Yongan Pharma. Co., Ltd., No. 2, Guangze Avenue, Economic Development Zone, Qianjiang City, Hubei Province, China 433132 SEM Minerals, L.P., 3806 Gardner Expressway, Quincy, IL 62305 Signo, LLC, 2000 S. Dairy Ashford Road, Suite 370, Houston, TX 77077 Stauber Holdings, Inc., f/k/a, Stauber Performance Ingredients, Inc., 4120 N. Palm Street, Fullerton, CA 92835– 1026 Shandong Xinhua Pharmaceutical USA, Inc., d/b/a SX Pharma, 2025 Mountain View Road, South El Monte, CA 91733 Uniprime International, LLC, 99 Corbett Way, Eatontown, NJ 07724 Wild Flavors, Inc., 1261 Pacific Avenue, Erlanger, KY 41018 (c) The Office of Unfair Import Investigations, U.S. International Trade Commission, 500 E Street SW, Suite 401, Washington, DC 20436; and (5) For the investigation so instituted, the Chief Administrative Law Judge, U.S. International Trade Commission, shall designate the presiding Administrative Law Judge. Responses to the complaint and the notice of investigation must be E:\FR\FM\06MRN1.SGM 06MRN1 8112 Federal Register / Vol. 84, No. 44 / Wednesday, March 6, 2019 / Notices submitted by the named respondents in accordance with section 210.13 of the Commission’s Rules of Practice and Procedure, 19 CFR 210.13. Pursuant to 19 CFR 201.16(e) and 210.13(a), such responses will be considered by the Commission if received not later than 20 days after the date of service by the Commission of the complaint and the notice of investigation. Extensions of time for submitting responses to the complaint and the notice of investigation will not be granted unless good cause therefor is shown. Failure of a 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 an initial determination and a final determination containing such findings, and may result in the issuance of an exclusion order or a cease and desist order or both directed against the respondent. By order of the Commission. Issued: February 28, 2019. Lisa Barton, Secretary to the Commission. [FR Doc. 2019–03988 Filed 3–5–19; 8:45 am] BILLING CODE 7020–02–P INTERNATIONAL TRADE COMMISSION [Investigation No. 337–TA–1145] Certain Botulinum Toxin Products, Processes for Manufacturing or Relating to Same and Certain Products Containing Same; Institution of Investigation U.S. International Trade Commission. ACTION: Notice. AGENCY: Notice is hereby given that a complaint was filed with the U.S. International Trade Commission on January 30, 2019, under section 337 of the Tariff Act of 1930, as amended, on behalf of Medytox Inc. of South Korea; Allergan plc of Ireland; Allergan, Inc., Irvine, California. Supplements to the complaint were filed on February 12, 2019, February 13, 2019, and February 14, 2019. The complaint alleges violations of section 337 based upon the importation into the United States, the sale for importation, and the sale within the United States after importation of SUMMARY: VerDate Sep<11>2014 18:35 Mar 05, 2019 Jkt 247001 certain botulinum toxin products, processes for manufacturing or relating to same and certain products containing same by reason of misappropriation of trade secrets, the threat or effect of which is to destroy or substantially injure a domestic industry in the United States. The complainants request that the Commission institute an investigation and, after the investigation, issue a limited exclusion order and cease and desist orders. ADDRESSES: The complaint, except for any confidential information contained therein, is 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: Pathenia M. Proctor, The Office of Unfair Import Investigations, U.S. International Trade Commission, telephone (202) 205–2560. SUPPLEMENTARY INFORMATION: Authority: The authority for institution of this investigation is contained in section 337 of the Tariff Act of 1930, as amended, 19 U.S.C. 1337, and in section 210.10 of the Commission’s Rules of Practice and Procedure, 19 CFR 210.10 (2018). Scope of Investigation: Having considered the complaint, the U.S. International Trade Commission, on February 28, 2019, ordered that— (1) Pursuant to 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)(A) of section 337 in the importation into the United States, the sale for importation, or the sale within the United States after importation of certain products identified in paragraph (2) by reason of misappropriation of trade secrets, the threat or effect of which is to destroy or substantially injure a domestic industry in the United States; PO 00000 Frm 00042 Fmt 4703 Sfmt 4703 (2) Pursuant to section 210.10(b)(1) of the Commission’s Rules of Practice and Procedure, 19 CFR 210.10(b)(1), the plain language description of the accused products or category of accused products, which defines the scope of the investigation, is botulinum neurotoxin products manufactured by Daewoong Pharmaceuticals Co., Ltd., specifically: (1) DWP–450 (prabotulinumtoxinA), variously marketed under the brand names Nabota®, JeuveauTM and other brand names; (2) products containing or derived from DWP–450; and (3) products containing or derived from the BTX strain assigned the high-risk pathogen control number 4–029–CBB– IS–001 by the Korean Centers for Disease Control and Prevention or the manufacturing process used to manufacture DWP–450; (3) 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: Medytox Inc., 626 Tehran Road, Gangnam, Seoul, South Korea; Allergan plc, Clonshaugh Business and Technology Park, Coolock, Dublin, D17 E400, Irland; Allergan, Inc., 2525 Dupont Drive, Irvine, CA 92612. (b) The respondents are the following entities alleged to be in violation of section 337, and are the parties upon which the complaint is to be served: Daewoong Pharmaceuticals Co., Ltd., Bongeunsaro 114-gil 12, Gangnam, Seoul, 06170; South Korea; Evolus, Inc., 17901 Von Karman Avenue, Suite 150, Irvine, CA 92614. (c) The Office of Unfair Import Investigations, U.S. International Trade Commission, 500 E Street SW, Suite 401, Washington, DC 20436; and (4) For the investigation so instituted, the Chief Administrative Law Judge, U.S. International Trade Commission, shall designate the presiding Administrative Law Judge. Responses to the complaint and the notice of investigation must be submitted by the named respondents in accordance with section 210.13 of the Commission’s Rules of Practice and Procedure, 19 CFR 210.13. Pursuant to 19 CFR 201.16(e) and 210.13(a), such responses will be considered by the Commission if received not later than 20 days after the date of service by the Commission of the complaint and the notice of investigation. Extensions of time for submitting responses to the complaint and the notice of investigation will not be granted unless good cause therefor is shown. Failure of a respondent to file a timely response to each allegation in the complaint and in this notice may be E:\FR\FM\06MRN1.SGM 06MRN1

Agencies

[Federal Register Volume 84, Number 44 (Wednesday, March 6, 2019)]
[Notices]
[Pages 8110-8112]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-03988]


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INTERNATIONAL TRADE COMMISSION

[Investigation No. 337-TA-1146]


Certain Taurine (2-Aminoethanesulfonic Acid), Methods of 
Production and Processes for Making the Same, and Products Containing 
the Same; Institution of Investigation

AGENCY: U.S. International Trade Commission.

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: Notice is hereby given that a complaint was filed with the 
U.S. International Trade Commission on January 30, 2019, under section 
337 of the Tariff Act of 1930, as amended, on behalf of Vitaworks IP, 
LLC of North Brunswick, New Jersey; Vitaworks, LLC of North Brunswick, 
New Jersey; and Dr. Songzhou Hu of North Brunswick, New Jersey. 
Supplemental exhibits were filed February 19, 2019. The complaint 
alleges violations of section 337 based upon the importation into the 
United States, the sale for importation, and the sale within the United 
States after importation of certain taurine (2-aminoethanesulfonic 
acid), methods of production and processes for making the same, and 
products containing the same by reason of infringement of certain 
claims of U.S. Patent No. 9,573,890 (``the '890 patent''); U.S. Patent 
No. 9,745,258 (``the '258 patent''); and U.S. Patent No. 10,040,755 
(``the '755 patent''). The complaint further alleges that an industry 
in the United States exists as required by the applicable Federal 
Statute.
    The complainants request that the Commission institute an 
investigation and, after the investigation, issue a limited exclusion 
order and cease and desist orders.

ADDRESSES: The complaint, except for any confidential information 
contained

[[Page 8111]]

therein, is 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: Pathenia M. Proctor, The Office of 
Unfair Import Investigations, U.S. International Trade Commission, 
telephone (202) 205-2560.

SUPPLEMENTARY INFORMATION: 
    Authority: The authority for institution of this investigation is 
contained in section 337 of the Tariff Act of 1930, as amended, 19 
U.S.C. 1337, and in section 210.10 of the Commission's Rules of 
Practice and Procedure, 19 CFR 210.10 (2018).
    Scope of Investigation: Having considered the complaint, the U.S. 
International Trade Commission, on February 28, 2019, 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, or the 
sale within the United States after importation of certain products 
identified in paragraph (2) by reason of infringement of one or more of 
claims 1 and 3-10 of the '890 patent; claims 1-3 of the '258 patent; 
and claims 1-9 of the '755 patent; and whether an industry in the 
United States exists as required by subsection (a)(2) of section 337;
    (2) Pursuant to section 210.10(b)(1) of the Commission's Rules of 
Practice and Procedure, 19 CFR 210.10(b)(1), the plain language 
description of the accused products or category of accused products, 
which defines the scope of the investigation, is ``taurine in its raw 
form, or combined with chemical additives such as an anti-caking agent, 
manufactured through processes featuring the use of alkali isethionate 
or ammonium isethionate'';
    (3) Pursuant to section 210.10(b)(3) of the Commission's Rules of 
Practice and Procedure, 19 CFR 210.10(b)(3), the presiding 
Administrative Law Judge shall hold an early evidentiary hearing, find 
facts, and issue an early decision, within 100 days of institution 
except for good cause shown, as to whether the complainants have 
satisfied the economic prong of the domestic industry requirement. 
Notwithstanding any Commission Rules to the contrary, which are hereby 
waived, any such decision should be issued in the form of an initial 
determination (ID) under Commission Rule 210.42(a)(3), 19 CFR 
210.42(a)(3). The ID will become the Commission's final determination 
30 days after the date of service of the ID unless the Commission 
determines to review the ID. Any such review will be conducted in 
accordance with Commission Rules 210.43, 210.44, and 210.45, 19 CFR 
210.43, 210.44, and 210.45. The issuance of an early ID finding that 
complainant does not satisfy the economic prong of the domestic 
industry requirement shall stay the investigation unless the Commission 
orders otherwise; any other decision shall not stay the investigation 
or delay the issuance of a final ID covering the other issues of the 
investigation;
    (4) 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:

Vitaworks IP, LLC, 195 Black Horse Lane, North Brunswick, NJ 08902
Vitaworks, LLC, 195 Black Horse Lane, North Brunswick, NJ 08902
Dr. Songzhou Hu, 195 Black Horse Lane, North Brunswick, NJ 08902

    (b) The respondents are the following entities alleged to be in 
violation of section 337, and are the parties upon which the complaint 
is to be served:

A to Z Nutrition, Inc., 14359 Miramar Parkway, Suite 218, Miramar, FL 
33027
Ampak Company, Inc., 1890 Palmer Avenue, Suite 301, Larchmont, NY 10538
Armada Nutrition LLC, 4637 Port Royal Road, Spring Hill, TN 37174
Atlantic Chemicals Trading of North America, Inc., 2 Oliver Street, 
Suite 602, Boston, MA 02109
Crossroad Ingredients LLC, 271 U.S. 46 West, Suite H206, Fairfield, NJ 
07004
Emote International, Inc., 1736 Wright Avenue, La Verne, CA 91750
Epikix, Inc., 6 Imperial Aisle, Irvine, CA 92606
Fuerst Day Lawson (USA), Ltd., Metropolitan Wharf, 70 Wapping Wall, 
London, England E1W 3SS, United Kingdom
Glanbia Nurtitional (NA), Inc., 2840 Loker Avenue East, Carlsbad, CA 
92101
Greating Shipping Co., 2225 W. Commonwealth Avenue, Suite 316, 
Alhambra, CA 91803
Green Wave Ingredients, Inc., 14821 Northam Street, La Mirada, CA 90638
Hard Eight Nutrition, LLC, 7511 Eastgate Road, Henderson, NV 89011
Fuchi Pharmaceutical Co., Ltd. d/b/a, Hubei Grand Life Science and 
Technology Co., Ltd., 12 Wangfen Road, Fuchi Town, Yangxin County, 
Hubei Province, China 435200
Jiangyin Huachang Food Additive Co., Ltd., No. 152, Yingbin West Road, 
Huangtu Town, JiangYin City, Jiang Su Province, China 214445
Natural Ingredient Corp., 155 N. Lake Avenue, 8th Floor, Suite 808, 
Pasadena, CA 91101
JSW Enterprises, LLC d/b/a, Nurtavative Ingredients, 600 Century 
Parkway, Suite 200, Allen, TX 75013
N.V.E., Inc. a/k/a, N.V.E. Pharmaceuticals, Inc., 15 Whitehall Road, 
Andover, NJ 07821
Pacific Rainbow International, Inc., 19905 Harrison Avenue, City of 
Industry, CA 91789
Pharmachem Laboratories, Inc., 265 Harrison Avenue, Kearny, NJ 07032
Prinova USA, LLC, 285 E. Fullerton Avenue, Carol Stream, IL 60188
Qianjiang Yongan Pharma. Co., Ltd., No. 2, Guangze Avenue, Economic 
Development Zone, Qianjiang City, Hubei Province, China 433132
SEM Minerals, L.P., 3806 Gardner Expressway, Quincy, IL 62305
Signo, LLC, 2000 S. Dairy Ashford Road, Suite 370, Houston, TX 77077
Stauber Holdings, Inc., f/k/a, Stauber Performance Ingredients, Inc., 
4120 N. Palm Street, Fullerton, CA 92835-1026
Shandong Xinhua Pharmaceutical USA, Inc., d/b/a SX Pharma, 2025 
Mountain View Road, South El Monte, CA 91733
Uniprime International, LLC, 99 Corbett Way, Eatontown, NJ 07724
Wild Flavors, Inc., 1261 Pacific Avenue, Erlanger, KY 41018

    (c) The Office of Unfair Import Investigations, U.S. International 
Trade Commission, 500 E Street SW, Suite 401, Washington, DC 20436; and
    (5) For the investigation so instituted, the Chief Administrative 
Law Judge, U.S. International Trade Commission, shall designate the 
presiding Administrative Law Judge.
    Responses to the complaint and the notice of investigation must be

[[Page 8112]]

submitted by the named respondents in accordance with section 210.13 of 
the Commission's Rules of Practice and Procedure, 19 CFR 210.13. 
Pursuant to 19 CFR 201.16(e) and 210.13(a), such responses will be 
considered by the Commission if received not later than 20 days after 
the date of service by the Commission of the complaint and the notice 
of investigation. Extensions of time for submitting responses to the 
complaint and the notice of investigation will not be granted unless 
good cause therefor is shown.
    Failure of a 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 an initial determination and a final determination containing 
such findings, and may result in the issuance of an exclusion order or 
a cease and desist order or both directed against the respondent.

    By order of the Commission.

    Issued: February 28, 2019.
Lisa Barton,
Secretary to the Commission.
[FR Doc. 2019-03988 Filed 3-5-19; 8:45 am]
BILLING CODE 7020-02-P