# ITI Manufacturing, Inc. – FDA Inspection, Jun 3, 2026

Source: https://www.keypedia.com/records/fda_inspections/iti-manufacturing-inc/1f150f2e-a4c4-4cb3-ab84-6b950b2a0012
Source feed: FDA_Inspections

> FDA inspection 1320202 of ITI Manufacturing, Inc., June 03, 2026. Classification: Voluntary Action Indicated (VAI). 4 citations. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1320202
- Company Name: ITI Manufacturing, Inc.
- Inspection Date: 2026-06-03
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 1182234 - 2022-10-28

## Related Officers

- [Investigator](https://www.keypedia.com/people/yuliana-hernandez-magana/450c3c39-02b7-489d-a710-e8c87c7657f4)

Company: https://www.keypedia.com/companies/iti-manufacturing-inc/7b3c5fc9-3826-4d59-a966-84fac511d0a3

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