# FDA Inspection 1280320 - Dane Technologies - August 25, 2025

Source: https://www.keypedia.com/records/fda_inspections/dane-technologies/d144259d-d1b9-4d9e-b83c-609671131780
Source feed: FDA_Inspections

> FDA Inspection 1280320 for Dane Technologies on August 25, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1280320
- Company Name: Dane Technologies
- Inspection Date: 2025-08-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Minneapolis District Office

## Related Documents

- [FDA Inspection 1280320 - 2025-08-25](https://www.keypedia.com/records/fda_inspections/dane-technologies/3c5fa92b-58eb-4a03-a101-46d039c53b75)
- [FDA Inspection 1165291 - 2022-03-18](https://www.keypedia.com/records/fda_inspections/dane-technologies/188e0845-80bf-4480-b81c-f3eada87894e)
- [FDA Inspection 1049814 - 2018-04-27](https://www.keypedia.com/records/fda_inspections/dane-technologies/cf20a6a9-86a2-42f9-b3e9-38f836487c9c)
- [FDA Inspection 1049814 - 2018-04-27](https://www.keypedia.com/records/fda_inspections/dane-technologies/29e47d32-6af8-4fd2-bc14-55347b8fda4f)
- [FDA Inspection 805861 - 2012-10-17](https://www.keypedia.com/records/fda_inspections/dane-technologies/8f7995ed-760b-4303-8811-dff98b114956)

Company: https://www.keypedia.com/companies/dane-technologies/81329829-4d98-4bcd-9a9f-bea75d18592e

Office: https://www.keypedia.com/offices/minneapolis-district-office/c79fc8dc-f884-48fc-ba80-2947f662511d