Main Number of warning letters received from ORA districts during the month CVM’s warning letter review ensures that the issued warning letter clearly follows the Agency’s rules, regulations and policies for the animal food/drug/device/biologics regulated industry and that these rules, regulations and policies are being implemented equally across all of the ORA district’s and internationally. Warning Letters are the Agency’s principal means of notifying the regulated industry of violations and achieving prompt voluntary correction. Warning letters need be issued soon after an inspection so the regulated industry is notified of their non-compliance. The regulated industry can then quickly implement corrective actions in order to become compliant with FDA’s rules, regulations and policies. <i>Information is current as of November 30, 2012</i> Number line 2012 FY 2012 Total: 72 2013 Fiscal Year Target FY 2013 YTD: 24 Main Number of warning letters reviewed and completed during the month Number column 2012 FY 2012 Total: 75 2013 Fiscal Year Target FY 2013 YTD: 17 Main Number of pending warning letters to be reviewed by CVM at the end of the month Number column 2012 FY 2012 Overall: 8 2013 Fiscal Year Target FY 2013 YTD: 15 http://www.fda.gov/AboutFDA/Transparency/track/ucm203425.htm FDA-TRACK CVM Dashboard ਍††਍਍਍਍਍਍਍