# Guidemia Technologies Inc. – FDA Inspection, Jul 6, 2026

Source: https://www.keypedia.com/records/fda_inspections/guidemia-technologies-inc/db5d20bc-23f8-4387-8e18-4f46d7dcf127
Source feed: FDA_Inspections

> FDA inspection 1325530 of Guidemia Technologies Inc., July 06, 2026. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 830. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1325530
- Company Name: Guidemia Technologies Inc.
- Inspection Date: 2026-07-06
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 1081235 - 2019-02-11
- [FDA Inspection 1021559 - 2017-07-03](https://www.keypedia.com/records/fda_inspections/guidemia-technologies-inc/30e549ec-ae05-4528-94a8-ff28886dd23b)
- [FDA Inspection 859270 - 2013-12-12](https://www.keypedia.com/records/fda_inspections/guidemia-technologies-inc/ff06699e-4f86-435c-8205-b3bdbee07fb2)

## Related Officers

- [Investigator](https://www.keypedia.com/people/jordan-i-abel/9cdc8877-ab20-4c0c-a17e-a8534d4f13f2)
- [Issuing Officer](https://www.keypedia.com/people/joseph-c-onyeike/cbd4ec5e-e545-4f3a-b0cb-d872af0fc2de)

Company: https://www.keypedia.com/companies/guidemia-technologies-inc/a4f32aed-30e9-49cb-a1e2-6efe08778b58

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