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483
•ARTVENTIVE MEDICAL GROUP, INC.•February 1, 2024

ARTVENTIVE MEDICAL GROUP, INC. – FDA 483, Feb 1, 2024

Record Details

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.

Company
ARTVENTIVE MEDICAL GROUP, INC.
Inspection date
February 1, 2024
Product type
device
Office
Division of Pharmaceutical Quality Operations IV
Person
  • Jenny L. Chisem
View Company Profile

ID · 2f874d53-1c03-4bdb-b211-59da1ac43df9

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370 Jay Street 7th Floor
Brooklyn, NY 11201
Scranton Office:
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