# FDA Inspection 1262638 - TOUL MEDITECH AB - February 27, 2025

Source: https://www.keypedia.com/records/fda_inspections/toul-meditech-ab/74e3e028-8974-4433-b8da-209fcef44945
Source feed: FDA_Inspections

> FDA Inspection 1262638 for TOUL MEDITECH AB on February 27, 2025. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1262638
- Company Name: TOUL MEDITECH AB
- Inspection Date: 2025-02-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1262638 - 2025-02-27](https://www.keypedia.com/records/fda_inspections/toul-meditech-ab/21d7a975-4736-40ab-815f-37a76ba389a5)
- [FDA Inspection 1262638 - 2025-02-27](https://www.keypedia.com/records/fda_inspections/toul-meditech-ab/4210053a-5ef9-4d99-bf24-87dedae32be3)
- [FDA Inspection 1262638 - 2025-02-27](https://www.keypedia.com/records/fda_inspections/toul-meditech-ab/ebf17d78-2935-4c36-b4f3-03d5b4785731)

Company: https://www.keypedia.com/companies/toul-meditech-ab/85995ffc-a020-4275-afac-cd320cdf114e

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