CHAMPIONSGATE, Fla., Dis. 9, 2010 / PRNewswire-USNewswire / - FDA Device Division, yomwe ikadali ndi nkhawa ndi poizoni wa mercury mu mano opangira mano ku America, ndi kuyitanitsanso kuwunika kwina kwa akatswiri zokhudzana ndi chitetezo. Kuphatikizika konsekonse kwa asayansi, mano ndi akatswiri azachipatala, motsogozedwa ndi International Academy of Oral Medicine and Toxicology (IAOMT) zikuyambitsa zovuta zatsopano ku gulu la Food and Drug Administration's (FDA) la Julayi'09 "zopanda ngozi" zamagulu amadzimadzi. Holiday Inn, Gaithersburg MD ndi tsamba la msonkhano wa FDA's Dental Products Panel Disembala 14 & 15 pomwe umboni wa asayansi ndi pagulu uperekedwe.
