# FDA Inspection 1243315 - SEKO MedTec Solutions - July 08, 2024

Source: https://www.keypedia.com/records/fda_inspections/seko-medtec-solutions/8f7f7d87-0dc8-4183-93e3-cb8446966bc2
Source feed: FDA_Inspections

> FDA Inspection 1243315 for SEKO MedTec Solutions on July 08, 2024. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1243315
- Company Name: SEKO MedTec Solutions
- Inspection Date: 2024-07-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1109811 - 2019-11-08](https://www.keypedia.com/records/fda_inspections/seko-medtec-solutions/d48bb3cb-241a-473b-8466-dfdbb2c88917)

Company: https://www.keypedia.com/companies/seko-medtec-solutions/fca64b51-c778-41c6-92b3-fe8e214800f7

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