3 laboratories in United States are accredited by A2LA under ISO/IEC 17025 to perform IEC 60335-2-80 testing. From the accredited scope text: “IEC 60335-2-80; EN 60335-2-80 Household and Similar Electrical Appliances: Particular Requirements for Fans IEC/EN 60601-1 Medical Electrical Equipment. Part 1: General Requirements for Safety and Ess” “IEC 60335-2-80; IEC 60335-2-99; EN 62233; IEC 62233; IEC 60335-2-37; IEC 60335-2-53; IEC 60335-2-23; IEC 60335-2-89; IEC 60335-2-64 On the following products or types of products: Industrial, Scientif” “IEC 60335-2-80:2015; IEC 60335-2-80:2002/A2:2008; EN 60335-2-80:2003/A2:2009; CSA 60335-2-80:17; IEC/EN/CSA 60335-2-80; IEC 60335-2-82:2017/A1:2020; IEC 60335-2-82:2002/A2:2015; EN 60335-2-82:2003/A2:”
Alpharetta, GA, US
IEC 60335-2-80:2015; IEC 60335-2-80:2002/A2:2008; EN 60335-2-80:2003/A2:2009; CSA 60335-2-80:17; IEC/EN/CSA 60335-2-80; IEC 60335-2-82:2017/A1:2020; IEC 60335-2-82:2002/A2:2015; EN 60335-2-82:2003/A2:2020; EN IEC 60335-2:2022; CS
Duluth, GA, US
IEC 60335-2-80; IEC 60335-2-99; EN 62233; IEC 62233; IEC 60335-2-37; IEC 60335-2-53; IEC 60335-2-23; IEC 60335-2-89; IEC 60335-2-64 On the following products or types of products: Industrial, Scientific, Medical (ISM), Informatio
Littleton, MA, US
IEC 60335-2-80; EN 60335-2-80 Household and Similar Electrical Appliances: Particular Requirements for Fans IEC/EN 60601-1 Medical Electrical Equipment. Part 1: General Requirements for Safety and Essential Performance IEC/EN 60601-
This page is a fixed slice of the register: every IEC 60335-2-80 scope we hold for United States. Search narrows it further by city, accreditation body, or a term from the scope text itself.
Search labs in United StatesAmerican Association for Laboratory Accreditation (A2LA) is the primary accreditation body issuing ISO/IEC 17025 accreditation for testing laboratories in United States.
ISO/IEC 17025 is the international standard for the competence of testing and calibration laboratories. Accreditation to this standard provides independent confirmation that a laboratory operates a quality management system and is technically competent to produce valid results within its declared scope.