12 laboratories in United States are accredited by A2LA under ISO/IEC 17025 to perform AOAC 996.08 testing. From the accredited scope text: “AOAC 996.08, 2004.03, 2011.03, 2013.01, AOAC-RI 020901, 071101 (Salmonella spp.) Enterobacteriaceae 8722, 160075 AOAC 2003.01, CMMEF Ch. 9 Escherichia coli and Coliforms 7806, 7811, 7812 AOAC 966.23,” “AOAC 996.08 METH-006 - Sample Enrichment for Salmonella spp. in Foods and Environmental Samples METH-009 - Detection of Salmonella using VIDAS Kube (SLM) E. coli 0157H7 by GENE-UP PCR (Screen only) AO” “AOAC 996.08, 2004.03 Salmonella – GENE-UP® Real-Time PCR QA-0010-0210 AOAC RI-121802 AOAC 2020.02 Salmonella – PCR (BAX) QA-0010-0180 AOAC RI-100201 AOAC 2003.09 Key: AOAC Association of Official Anal” “AOAC 996.08, 2004.03 Salmonella – ELFA (VIDAS UP) QA-0010-0190 AOAC 2013.01, AOAC RI-071101 Salmonella – GENE-UP® Real-Time PCR QA-0010-0210 AOAC 2020.02, AOAC RI-121802 Salmonella – PCR (BAX) QA-0010”
Arlington, TX, US
AOAC 996.08, 2004.03 Salmonella – GENE-UP® Real-Time PCR QA-0010-0210 AOAC RI-121802 AOAC 2020.02 Salmonella – PCR (BAX) QA-0010-0180 AOAC RI-100201 AOAC 2003.09 Key: AOAC Association of Official Analytical Chemists International
NMSU Campus Las Cruces, NM, US
AOAC 996.08 METH-006 - Sample Enrichment for Salmonella spp. in Foods and Environmental Samples METH-009 - Detection of Salmonella using VIDAS Kube (SLM) E. coli 0157H7 by GENE-UP PCR (Screen only) AOAC 2019.03 METH-031 - GENE-U
Cypress, CA, US
Test Method Name In-House Method Reference Method(s) Listeria spp. – ELFA (VIDAS UP) QA-0116-4100 AOAC 2013.10 Listeria spp. – PCR (BAX) QA-0116-4086 AOAC RI-030502 Listeria spp. and L. monocytogenes – ELFA (VIDAS) QA-0116-4088 AOAC 20
Amarillo, TX, US
AOAC 996.08, 2004.03 Salmonella – ELFA (VIDAS UP) QA-0010-0190 AOAC 2013.01, AOAC RI-071101 Salmonella – GENE-UP® Real-Time PCR QA-0010-0210 AOAC 2020.02, AOAC RI-121802 Salmonella – PCR (BAX) QA-0010-0180 AOAC 2003.09, AOA
Springfield, MO, US
AOAC 996.08, 2004.03 Salmonella GENE-UP® Real-Time PCR QA-0010-0210 AOAC 2020.02 AOAC RI-121802 Salmonella PCR (BAX) QA-0010-0180 AOAC 2003.09 AOAC RI 100201 Salmonella PCR Real Time ABAX PCR QA-0010-0185 AOAC 2013.02 AOAC RI 08120
Madison, WI, US
Test Method Name In-House Method Reference Method(s) GENE-UP® enviroPRO™ Real-Time PCR for the Detection of Salmonella and Listeria spp. QA-0010-0510 AOAC RI-061801 Listeria monocytogenes – Automated BAX® Real-Time PCR QA-0116-4120 AO
Turlock, CA, US
AOAC 996.08, 2004.03, 2011.03, 2013.01, AOAC-RI 020901, 071101 (Salmonella spp.) Enterobacteriaceae 8722, 160075 AOAC 2003.01, CMMEF Ch. 9 Escherichia coli and Coliforms 7806, 7811, 7812 AOAC 966.23, 966.24, CMMEF Ch. 9, FDA BAM Ch. 4
Salida, CA, US
Test Method Name In-House Method Reference Method(s) E. coli (VRB) QA-0025-0304 FDA BAM Ch.4 CMMEF 9.93 SMEDP 7.040 E. coli/g (Petrifilm™) QA-0025-0375 SMEDP 7.070 AOAC 991.14, 998.08 Lactics (Petrifilm™) QA-0040-2000 AOAC RI-041701
Minnetonka, MN, US
Test Method Name In-House Method Reference Method(s) Enterobacteriaceae/g QA-0017-0220 CMMEF 9.6.2 Escherichia coli (MPN) QA-0025-0302 AOAC 966.24, FDA BAM Ch. 4, SMEWW (22nd Ed.) E. coli (VRB) QA-0025-0304 FDA BAM Ch. 4 E. coli/g (
Stone Mountain, GA, US
AOAC 996.08, 2004.03 Salmonella – ELFA (VIDAS UP) QA-0010-0190 AOAC 2013.01 AOAC RI-071101 Salmonella (GENE-UP® Real-Time PCR) QA-0010-0210 AOAC 2020.02 AOAC RI-121802 Salmonella – PCR (BAX) QA-0010-0180 AOAC 2003.09 AOAC RI-100201
Columbus, OH, US
AOAC 996.08, AOAC 2004.03 (Salmonella spp.) 32.2 10058 AOAC 2011.03 (EZ Salmonella spp.) 32.3 10058 AOAC 2013.01, AOAC-RI 071101, USDA MLG Chapter 4 (Salmonella spp. UP) 33.1 10058 AOAC 2004.02, USDA MLG Chapter 8 (Liste
Columbus, OH, US
Qualitative Test Method Name In-House Method Reference Method(s) E. coli O157 (Including: H7) – ELFA (VIDAS UP) QA-0025-0325 AOAC RI-060903 E. coli O157:H7 – Automated BAX Real-Time PCR QA-0025-0820 AOAC RI-031002 Listeria monocytoge
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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.