Lin Zhi International
Biotechnology, 2945 Oakmead VLG Ct, Santa Clara, California, 95051, United States, 11-50 Employees
Phone Number: 40**********
Who is LIN-ZHI INTERNATIONAL
Lin-Zhi International, Inc. (LZI), located in Santa Clara, California, is a biotechnology company that has been in business since 1998. LZI specializes in the research, development, and m...
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Headquarters: 2945 Oakmead VLG Ct, Santa Clara, California, 95051, United States
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Date Founded: 1998
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Employees: 11-50
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Revenue: $25 Million to $50 Million
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Active Tech Stack: See technologies
Industry: Biotechnology
SIC Code: 5047
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Frequently Asked Questions Regarding Lin-Zhi International
Answer: Lin-Zhi International's headquarters are located at 2945 Oakmead VLG Ct, Santa Clara, California, 95051, United States
Answer: Lin-Zhi International's phone number is 40**********
Answer: Lin-Zhi International's official website is https://lin-zhi.com
Answer: Lin-Zhi International's revenue is $25 Million to $50 Million
Answer: Lin-Zhi International's SIC: 5047
Answer: Lin-Zhi International has 11-50 employees
Answer: Lin-Zhi International is in Biotechnology
Answer: Lin-Zhi International top competitors include: Gilead Sciences , ProteinSimple , Thermo Fisher Scientific
Answer: Lin-Zhi International contact info: Phone number: 40********** Website: https://lin-zhi.com
Answer: Lin-Zhi International, Inc. (LZI), located in Santa Clara, California, is a biotechnology company that has been in business since 1998. LZI specializes in the research, development, and manufacturing of in vitro diagnostic reagents for drugs of abuse. LZI is dedicated to the development of innovative and quality products for clinical diagnostics. Lin-Zhi International, Inc.s pledge to our customers is to deliver high quality in vitro diagnostic medical devices that meet or exceed their expectations. We strive to provide qualified technical support and attentive, professional customer service. There are several business aspects that play a role into the company including the manufacturing process, products, quality control, and customer interactions. All those aspects are required to be first rate, supplemented with thorough, traceable documentation, and produced under good manufacturing processes (GMP), ISO 13485:2003 (International Organization for Standardization for medical device quality management system requirements), 21 CFR 820 (quality system regulation for medical devices), the European Unions In Vitro Diagnostic Directive IVDD 98/79/EC, and Canadian Medical Devices Conformity Assessment System (CMDCAS SOR/98-282). Since the medical device industry is well regulated, the safety and efficacy of our Quality Management System (QMS) and devices are high priority. In conclusion, as part our commitment to excellence, we seek to continually improve our QMS and products.
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