# FDA Inspection 1325530 - Guidemia Technologies Inc. - July 06, 2026

Source: https://www.keypedia.com/records/fda_inspections/guidemia-technologies-inc/b9ee86e5-b6b4-4bde-96b8-8996d33efa5a
Source feed: FDA_Inspections

> FDA Inspection 1325530 for Guidemia Technologies Inc. on July 06, 2026. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1325530 - 2026-07-06](https://www.keypedia.com/records/fda_inspections/guidemia-technologies-inc/db5d20bc-23f8-4387-8e18-4f46d7dcf127)
- [FDA Inspection 1081235 - 2019-02-11](https://www.keypedia.com/records/fda_inspections/guidemia-technologies-inc/15837754-2496-4f59-9fb2-b1ac07784071)
- [FDA Inspection 859270 - 2013-12-12](https://www.keypedia.com/records/fda_inspections/guidemia-technologies-inc/ff06699e-4f86-435c-8205-b3bdbee07fb2)
- [FDA Inspection 859270 - 2013-12-12](https://www.keypedia.com/records/fda_inspections/guidemia-technologies-inc/f1a5b43d-b2a5-4a0a-8818-a520b096655a)

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