According to the announcement of the State Food and Drug Administration on the regulation of business behaviors in the field of medical device circulation and the work plan of Hunan Province for the regulation of business behaviors in the field of medical device circulation, the food and drug administration departments at all levels in our province conscientiously organized and urged the medical device trading enterprises under their jurisdiction to carry out self-inspection and rectification work. As of July 15, 2016, 8,732 of the province's 9,272 medical device business enterprises had conducted self-inspection and rectification and submitted self-inspection and rectification reports in accordance with regulations, while 540 had not submitted self-inspection and rectification reports in accordance with regulations. The relevant municipal Food and Drug Administration in accordance with the requirements of the jurisdiction did not submit a self-inspection and rectification report of the medical device business enterprises were publicized.
Please refer to the attachment for the list of medical device business enterprises that failed to submit self-inspection and rectification reports as required.
Post time: Jun-03-2023