# FDA Inspection 1267866 - VENOKA USA INC - April 25, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/venoka-usa-inc/8e28e624-5f67-4913-b9d6-470ed01077cd
Source feed: FDA_Inspections

> FDA Inspection 1267866 for VENOKA USA INC on April 25, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1267866
- Company Name: VENOKA USA INC
- Inspection Date: 2025-04-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1267866 - 2025-04-25](https://www.globalkeysolutions.net/records/fda_inspections/venoka-usa-inc/d3f6f5ea-5e86-43cd-9fa1-32a5966382b4)
- [FDA Inspection 1267866 - 2025-04-25](https://www.globalkeysolutions.net/records/fda_inspections/venoka-usa-inc/1045714b-898b-4e76-a5bc-4445dc6479eb)
- [FDA Inspection 1267866 - 2025-04-25](https://www.globalkeysolutions.net/records/fda_inspections/venoka-usa-inc/5f7121a4-0e7f-4f2a-86aa-1fe034bfa6fc)

Company: https://www.globalkeysolutions.net/companies/venoka-usa-inc/d994397d-55d1-4180-972c-7f8c103469b3

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