FDA 483 - ARTVENTIVE MEDICAL GROUP, INC. - February 01, 2024

ARTVENTIVE MEDICAL GROUP, INC. in San Marcos, CA, was inspected from January 31 to February 1, 2024. The inspection revealed one observation concerning the firm's failure to provide required medical device information to the Global Unique Device Identification Database (GUDID). This indicates a deficiency in regulatory compliance regarding device identification data submission.