# TIA – FDA Inspection, Feb 11, 2026

Source: https://www.keypedia.com/records/fda_inspections/tia/9ec07d3a-1c20-477b-9006-f639ad79a9ae
Source feed: FDA_Inspections

> FDA inspection 1302350 of TIA, February 11, 2026. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 801 and 803. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1302350
- Company Name: TIA
- Inspection Date: 2026-02-11
- 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: 3

## Related Documents

- FDA Inspection 1306798 - 2026-03-09
- FDA Inspection 1277479 - 2025-07-15
- FDA Inspection 1262952 - 2025-02-21
- FDA Inspection 1224865 - 2023-11-16

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/jocelyn-c-turner/7e39f6e0-9750-4460-8a4e-27ee9306b77e)

Company: https://www.keypedia.com/companies/tia/13d724b0-631e-469c-8dd6-082b24280fad

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