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Special rectification
Source: | Author:pmoc93090 | Published time: 1777 days ago | 1538 Views | Share:
  On March 17, 2014, the State Food and Drug Administration held a press conference. From now on, the State Food and Drug Administration will carry out a five-month "five remediation" special action for medical devices in the country, focusing on five behaviors: false registration and declaration of medical devices, illegal production, illegal operation, expansion of publicity and use of unlicensed products. The special action takes the key products, key enterprises and key case clues as the breakthrough point, through the combination of secret investigation, centralized investigation and surprise inspection, to crack down on illegal behaviors and further standardize the market order.
  According to the requirements of the State Food and drug administration, if any illegal act is found in the special action, it shall be dealt with promptly, strictly and seriously, and punished according to the upper limit prescribed by laws and regulations; if the case is serious, the license of the manufacturer, operator and product shall be revoked; if any crime is suspected, it shall be transferred to the public security organ for criminal responsibility according to law; for any product with potential safety hazard, it shall be dealt with promptly and severely Stop the sale and use, order the enterprise to recall and supervise the destruction.