483
MECTA CorporationFDA 483 - MECTA Corporation - September 01, 2009
Record Details
Mecta Corporation in Tualatin, OR, was inspected by the FDA from August to September 2009. The inspection revealed a significant issue regarding medical device reporting. Specifically, the firm failed to submit a timely Medical Device Report (MDR) after becoming aware of a patient's death following treatment with their Spectrum 5000Q device.
Open in Dashboard
ID · d3557811-7265-4502-9987-7e45e5f87475