www.fdanews.com/articles/164408-fujinon-handed-form-483-on-capa-complaint-handling-issues

Fujinon Handed Form 483 on CAPA, Complaint-Handling Issues

May 9, 2014

Wayne, N.J., devicemaker Fujinon received a three-observation Form 483 for CAPA failures and other quality system issues.
The GMP Report