# Tricor Systems – FDA Inspection, Mar 8, 2023

Source: https://www.keypedia.com/records/fda_inspections/tricor-systems/bff37e39-710e-4225-becc-36d60036aa5b
Source feed: FDA_Inspections

> FDA inspection 1199278 of Tricor Systems, March 08, 2023. Classification: Voluntary Action Indicated (VAI). 8 citations under 21 CFR parts 803 and 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1199278
- Company Name: Tricor Systems
- Inspection Date: 2023-03-08
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 8

## Related Documents

- FDA Inspection 928462 - 2015-05-21
- FDA Inspection 711086 - 2011-02-24
- [FDA Inspection 554108 - 2008-10-09](https://www.keypedia.com/records/fda_inspections/tricor-systems/dcf5819c-a7a1-4db4-b51e-ebba272d2f93)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/jesse-a-vazquez/cac5b170-d0ea-4355-af5d-3d81546ff0fe)

Company: https://www.keypedia.com/companies/tricor-systems/180344dc-f890-42f4-9023-6c911ed1ff15

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7