How to report medical equipment illegal enterprises

Reporters from the city Food and Drug Administration was informed that, in order to further standardize the city's medical device production enterprises production order, crack down on violations, from now on to the end of October, the Bureau will carry out special inspection of medical device production enterprises in the city. The public found that medical device manufacturers have violations, you can call 12331 complaint report.

The special inspection will focus on checking whether the medical device manufacturers based on the "Good Manufacturing Practice for Medical Devices" to establish a quality management system; whether the quality management system is in place; whether the procurement, production, inspection, sales records are complete; inspection instruments and equipment, product testing and other aspects of compliance with standards. At the same time will be a comprehensive investigation of the production of quality risks and safety hazards, and crack down on illegal behavior. It is reported that the regulatory authorities will investigate and deal with violations of the law, destroyed a number of illegal production "black spot", exposure of a number of illegal enterprises. Municipal Food and Drug Administration will form a supervisory inspection team and from time to time on the districts, counties (cities) Bureau, Development Zone sub-bureau under the jurisdiction of the inspection of production enterprises to supervise, and the results will be included in the end of the year evaluation of the supervision of medical devices.