Unqualified medical device products will be traced throughout the whole process
A few days ago, the State Administration for Market Regulation, the National Development and Reform Commission, the Ministry of Industry and Information Technology, the Ministry of Public Security, the Ministry of Commerce, the General Administration of Customs, and the Food and Drug Administration jointly issued a notice on the “National Anti-epidemic Material Product Quality and Market Order Special Rectification Action Plan”. Relevant departments in all regions of the country carried out rectification actions.
The rectification is the whole process, which will run through the entire chain of supervision of the production, circulation, consumption, and export of epidemic prevention materials. The source of production, corporate qualifications, product standards, and product quality will be checked.
At the same time, the entire process of unqualified products will be traced, producers and operators will be held accountable according to law, and the quality of epidemic prevention materials will be strictly checked.