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TUV USA, Inc.

Accredited by: ANAB

TÜV USA, Inc. is a certification body that provides testing, inspection, and certification services across various industries. They focus on ensuring compliance with safety, quality, and performance standards for products and systems. Their services include product certification, management system certification, and training, aimed at enhancing operational efficiency and market access for businesses. TÜV USA operates under the global TÜV Rheinland Group, which is recognized for its expertise in technical services.

http://www.tuv-usa.com

215 Main Street, Salem, NH 03079, United States

Certification Scopes (2)

ISO 9001

Certification Body for Management Systems

ANSI National Accreditation Board

United States of America

TUV USA, Inc. holds an Accreditation ID of MS-8240, issued by the ANSI National Accreditation Board, confirming its compliance with ISO/IEC 17021-1 for management systems certification. The accreditation covers various standards, including ISO 9001 for quality management systems and ISO 13485 for medical device management systems, with specific scopes across multiple economic sectors such as textiles, aerospace, and medical devices. The accreditation is valid from August 1, 1995, until August 1, 2030, and can be verified through ANAB.

Manufacture of basic pharmaceutical products and pharmaceutical preparations
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ISO 9001

Certification Body for Management Systems

ANSI National Accreditation Board

United States of America

TUV USA, Inc. holds an Accreditation ID MS-8240 from the ANSI National Accreditation Board, confirming its compliance with ISO/IEC 17021-1 for management system audits and certifications. The accreditation covers various standards, including ISO 9001 for quality management and ISO 13485 for medical device management systems, with specific scopes across multiple economic sectors such as textiles, aerospace, and medical devices. This accreditation is valid from 01 August 1995 and will expire on 01 August 2030, with the latest updates reflecting changes in standards as of 2025.

Manufacture of basic pharmaceutical products and pharmaceutical preparations
View Source