Czech Company's Medical Devices Subject to Import Refusal After FDA Finds MDR, CGMP ViolationsDecember 27, 2012 by Brian Feito|FDA
FDA Now Accepting Electronic Submission of Laboratory Analyses, Plans to Automate ReviewsDecember 21, 2012 by Tim Warren|FDA
FDA Enforcement Report on Recalls & Field Corrections for Dec. 19December 20, 2012 by Brian Feito|FDA