# Tricor Systems – FDA Inspection, Oct 9, 2008

Source: https://www.keypedia.com/records/fda_inspections/tricor-systems/dcf5819c-a7a1-4db4-b51e-ebba272d2f93
Source feed: FDA_Inspections

> FDA inspection 554108 of Tricor Systems, October 09, 2008. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 554108
- Company Name: Tricor Systems
- Inspection Date: 2008-10-09
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- [FDA Inspection 1199278 - 2023-03-08](https://www.keypedia.com/records/fda_inspections/tricor-systems/bff37e39-710e-4225-becc-36d60036aa5b)
- FDA Inspection 928462 - 2015-05-21
- FDA Inspection 711086 - 2011-02-24

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