Visit A&G at MedTec, 4 – 6 April, 2017 – Messe-Stuttgart, Germany, booth 1K16 (map available here)
FDA inspection passed at 26.01.2017, full inspection was performed at 23-26.01.20.17, 2 FDA-483 Inspectional Observations was issued.
19-20.12.2016 A&G cleanroom revalidation was performed by Zeus Tech Oy, according to ISO14644-1:2000 – operational class 7.
A&G had at 2016 next audits: 18.04.2016 factory inspection by SGS Fimko Oy; 25.05.2016 EHS audit by GEHC and Intertek Certification France;
A&G will participate in Compamed 2016 in Düsseldorf, visit us in united stand 8aN35! See you in Compamed!
The primary characteristic of our quality policy is our adherence to the integrated quality system (ISO 9001, ISO 13485, ISO 14001, OHSAS 18001)
A&G passed cleanroom validation at the end of 2015 by Zeus Tech OY. According to ISO14644-1:2000 – operational class 7.
FDA inspection passed at 29.01.13. No FDA-483 Inspectional Observations was issued and no verbal observations were discussed.
Visit A&G at MedTec Stuttgart, 12-14.04.2016, booth 5E13.