# FDA Inspection 1239270 - PATHWAY MEDTECH, LLC - May 22, 2024

Source: https://www.keypedia.com/records/fda_inspections/pathway-medtech-llc/6baf05b6-eec2-403e-ad6c-65217e14c0c5
Source feed: FDA_Inspections

> FDA Inspection 1239270 for PATHWAY MEDTECH, LLC on May 22, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1239270
- Company Name: PATHWAY MEDTECH, LLC
- Inspection Date: 2024-05-22
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1239270 - 2024-05-22](https://www.keypedia.com/records/fda_inspections/pathway-medtech-llc/fa2c1e3d-2e6b-47e8-a755-1b7c8bc7edb0)
- [FDA Inspection 1062131 - 2018-08-03](https://www.keypedia.com/records/fda_inspections/pathway-medtech-llc/506b3f9d-95e6-4473-b21c-5188e6572c99)

Company: https://www.keypedia.com/companies/pathway-medtech-llc/d5f51318-f0f1-4c50-b5b5-f56952cb5577

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