Home > Newsletters > FDAnews Device Daily Bulletin > California Devicemaker Warned By FDA on Numerous GMP Lapses
FDAnews Device Daily Bulletin
July 20, 2012 | Vol. 9 No. 142
California Devicemaker Warned By FDA on Numerous GMP Lapses
An optical supplies manufacturer has received an FDA warning letter for nine violations, most relating to complaint handling, device design and process control procedures. The letter to American Optisurgical (AOI) from the FDA’s Los Angeles District Office is dated June 14 and follows a Jan. 30-Feb. 23 inspection of the company’s Lake Forest, Calif., plant.
Devices & Diagnostics Letter
ePublishing :: CMS, Hosting & Web Development | © Copyright by FDAnewsAll rights reserved. Do not duplicate or redistribute in any form.