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

Source: https://www.globalkeysolutions.net/records/483/artventive-medical-group-inc/2f874d53-1c03-4bdb-b211-59da1ac43df9

> FDA 483 for ARTVENTIVE MEDICAL GROUP, INC. on February 01, 2024. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: ARTVENTIVE MEDICAL GROUP, INC.
- Inspection Date: 2024-02-01
- Product Type: device
- Office Name: Division of Pharmaceutical Quality Operations IV
- Summary: 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.

## Related Officers

- [Jenny L. Chisem](https://www.globalkeysolutions.net/people/jenny-l-chisem/d9c3fada-4f08-4f1a-9c6c-06a3c521534c)

Company: https://www.globalkeysolutions.net/companies/artventive-medical-group-inc/1566530c-3ac2-4571-976b-84f8a8466ed4

Office: https://www.globalkeysolutions.net/offices/division-of-pharmaceutical-quality-operations-iv/a2d2ff91-dc0f-433e-b91f-ca90ff8998b6