# FDA 483 - Angiodynamics, Inc. - January 10, 2025

Source: https://www.keypedia.com/records/483/angiodynamics-inc/68879050-0f6c-4eb5-9185-7ec762c34b2c

> FDA 483 for Angiodynamics, Inc. on January 10, 2025. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Angiodynamics, Inc.
- Inspection Date: 2025-01-10
- Product Type: device
- Office Name: New York District Office
- Summary: Angiodynamics, Inc. in Queensbury, NY, a medical device manufacturer, was cited for deficiencies in its complaint handling system during an FDA inspection. The firm's procedures for receiving and evaluating complaints were found to be inadequate, with numerous instances of delayed documentation. Additionally, records of complaint investigations lacked required information, specifically the dates of the investigations.

## Related Documents

- [483 - Unknown Date](https://www.keypedia.com/records/483/angiodynamics-inc/b4ef8e8e-4da7-46ed-83df-1b55213cd54d)

## Related Officers

- [investigator](https://www.keypedia.com/people/wendy-m-stone/715b04f5-3949-4ca6-9bda-26ff611e9354)

Company: https://www.keypedia.com/companies/angiodynamics-inc/cabf05c2-1177-4dba-93a3-ba8e56e956d6

Office: https://www.keypedia.com/offices/new-york-district-office/9fa3d265-16ca-438d-8a6e-b47f60dc260d