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GMW 3172 Accredited Testing Labs in United States

4 laboratories in United States are accredited by A2LA under ISO/IEC 17025 to perform GMW 3172 testing. Most frequently tested analytes via this method in United States: Ozone, Voltage. Accredited providers include Element Materials Technology Detroit – Warren 11 Mile, TUV Rheinland (Suzhou) Co.,, Element Materials Technology Kokomo, MGA Research Corporation. Sites located in Warren, MI, Taicang City, Jiangsu, Kokomo, IN, Burlington, WI.

Labs
4
Top matrix
Top analyte
Ozone
1 labs
Primary AB
A2LA
4 labs

Accredited Labs

Element Materials Technology Detroit – Warren 11 Mile
Warren, MI, US

(A2LA Cert. No. 0098.12 (Formerly 0038.03)) Revised 02/03/2026 Page 2 of 2 Parameter Range Test Method Voltage – AC – Measure2 100 μV to 15 kV MIL-STD-202-301 AC – Generate2 100 mV to 10 V @ 1Hz to 30 MHz, 10V to 40V @ 1 Hz to 1.3 M

TUV Rheinland (Suzhou) Co.,
Taicang City, Jiangsu, US

(A2LA Cert. No. 4301.05) 07/31/2025 Page 5 of 7 Test Technology Test Method(s) 1: Ozone Test IEC 60811-403; DIN EN ISO 1431-1; DIN 53509-1; ISO 19642; ISO 6722; VW 60360; VW 60306; MBN LV 112-1; MBN LV 112-2; MBN LV 112-4;

Element Materials Technology Kokomo
Kokomo, IN, US

(A2LA Cert. No. 1123.07) Revised 06/05/2025 Page 3 of 3 Test Type Test Parameters Test Method/Standard Vibration Test Fixture1 Transmissibility Frequency: 5 Hz to 2,500 Hz GMW 3172 1 Also using customer sp

MGA Research Corporation
Burlington, WI, US

(A2LA Cert. No. 0850.03) Revised 05/28/2025 Page 1 of 4 SCOPE OF ACCREDITATION TO ISO/IEC 17025:2017 MGA RESEARCH CORPORATION 855 Britannia Road East Mis

Top analytes for GMW 3172 in United States

  • Ozone (1)
  • Voltage (1)

About ISO/IEC 17025 in United States

American 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.

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