# FDA Inspection 1286118 - Splintek, Inc - October 30, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/splintek-inc/db3a8395-f03a-4b50-83b3-a3305b38fa92
Source feed: FDA_Inspections

> FDA Inspection 1286118 for Splintek, Inc on October 30, 2025. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1286118
- Company Name: Splintek, Inc
- Inspection Date: 2025-10-30
- 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 1286118 - 2025-10-30](https://www.globalkeysolutions.net/records/fda_inspections/splintek-inc/1a2a87c3-1afb-42a4-b6ea-b49f0774c8d8)
- [FDA Inspection 1286118 - 2025-10-30](https://www.globalkeysolutions.net/records/fda_inspections/splintek-inc/6f08ce17-e4f2-46a5-9c65-b67deec186a0)
- [FDA Inspection 1286118 - 2025-10-30](https://www.globalkeysolutions.net/records/fda_inspections/splintek-inc/e9e7129c-b82d-4e11-8522-b0754e0e443f)
- [FDA Inspection 965812 - 2016-02-05](https://www.globalkeysolutions.net/records/fda_inspections/splintek-inc/7bc911b3-f05c-4809-8aa5-e780dab6964f)
- [FDA Inspection 965812 - 2016-02-05](https://www.globalkeysolutions.net/records/fda_inspections/splintek-inc/6172220a-e7aa-4e05-a780-fe56c4fe9040)

Company: https://www.globalkeysolutions.net/companies/splintek-inc/97a92bf8-e674-4299-be52-66b7b20cb5f5

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