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On March 10, the website of the State Food and Drug Administration issued a notice calling on all localities to carry out the "five rectifications" of medical devices by the end of June this year.
Since March 15, 2014, the State Administration of Food and Drug Administration has launched a nationwide "five rectifications" of medical devices, focusing on five illegal acts of false registration and declaration, illegal production, illegal operation, exaggerated publicity and the use of undocumented products.
The State Administration of Food and Drug Administration requires that, during the "look back" period, all localities should focus on checking whether the risks identified by the special action, whether the unqualified products found have been disposed of accordingly, whether corrective measures have been formulated, whether the rectification or punishment measures have been implemented; (Health News)