# FDA 483 - AVID Medical, Inc. - December 05, 2022

Source: https://www.keypedia.com/records/483/avid-medical-inc/0c422536-70b3-48fd-92dc-0fe697e446b4

> FDA 483 for AVID Medical, Inc. on December 05, 2022. Product: device. Access full analysis and detailed observations.

---

## Details

- Record Type: 483
- Company Name: AVID Medical, Inc.
- Inspection Date: 2022-12-05
- Product Type: device
- Office Name: Office of Regulatory Affairs
- Summary: AVID Medical, Inc. in Toano, VA, was inspected by the FDA, revealing significant issues with quality system procedures. The inspection found failures in establishing adequate procedures for in-process product acceptance, controlling non-conforming products, and ensuring routine equipment calibration and maintenance. These observations indicate a lack of adherence to established quality control processes.

## Related Officers

- [Tiki Dixon](https://www.keypedia.com/people/tiki-dixon/b3160a2c-ef16-4fa2-b9b9-4c3a0ed17c5b)

Company: https://www.keypedia.com/companies/avid-medical-inc/9b55cc45-2b4c-41ed-b8cd-668a63bfcd9c

Office: https://www.keypedia.com/offices/office-of-regulatory-affairs/ff91c598-cf72-4dbe-a2c8-7519c64cbc64