Posted on 6/29/2022
Shenzhen Viatom Technology Co., Ltd completed the Medical Device Single Audit Program and obtained the MDSAP certificate issued by Technischer Überwachungs-Verein.
MDSAP certification is an audit process initiated by AMDRF, based on ISO 13485, recognized and joined by regulatory agencies in the United States (FDA), Australia (TGA), Brazil (ANVISA), Canada (HC), and Japan (MHLW). Aim to establish a single audit process that meets and unifies the audit requirements of the above-mentioned countries, making the audit more comprehensiv...