# FDA Inspection 1320182 - Vekor Medical, Inc. - May 12, 2026

Source: https://www.keypedia.com/records/fda_inspections/vekor-medical-inc/c65f47a5-02e4-48de-9f47-a73a28307241
Source feed: FDA_Inspections

> FDA Inspection 1320182 for Vekor Medical, Inc. on May 12, 2026. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1320182
- Company Name: Vekor Medical, Inc.
- Inspection Date: 2026-05-12
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1234369 - 2024-03-07](https://www.keypedia.com/records/fda_inspections/vekor-medical-inc/6616bd0f-532d-4175-8334-f9dd3f8192e7)

Company: https://www.keypedia.com/companies/vekor-medical-inc/c23211a6-2d23-4f7f-8256-d9e74c14d7db

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