# Trillium Technology, Inc. – FDA Inspection, Apr 30, 2018

Source: https://www.keypedia.com/records/fda_inspections/trillium-technology-inc/1de373ef-d0e5-4ffa-9283-7aa47aec5bbc
Source feed: FDA_Inspections

> FDA inspection 1050135 of Trillium Technology, Inc., April 30, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1050135
- Company Name: Trillium Technology, Inc.
- Inspection Date: 2018-04-30
- 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: 2

## Related Documents

- [FDA Inspection 911428 - 2015-01-30](https://www.keypedia.com/records/fda_inspections/trillium-technology-inc/52a45566-53e3-422c-8034-f52de788c708)
- FDA Inspection 838130 - 2013-06-28
- [FDA Inspection 745386 - 2011-09-20](https://www.keypedia.com/records/fda_inspections/trillium-technology-inc/07c517d6-6ddc-4acf-a7b5-74819b5aac87)

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/trillium-technology-inc/21fc5f7e-190c-4776-a402-969ea81d40ae

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