# FDA Inspection 1263719 - Cornelis Verhoef, MD - February 14, 2025

Source: https://www.keypedia.com/records/fda_inspections/cornelis-verhoef-md/34181bcd-1975-49cd-aee4-f421ed3792f5
Source feed: FDA_Inspections

> FDA Inspection 1263719 for Cornelis Verhoef, MD on February 14, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1263719
- Company Name: Cornelis Verhoef, MD
- Inspection Date: 2025-02-14
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1263719 - 2025-02-14](https://www.keypedia.com/records/fda_inspections/cornelis-verhoef-md/7c5a838e-2ad6-49f7-aad3-47880afdb796)

Company: https://www.keypedia.com/companies/cornelis-verhoef-md/60a85a5f-21eb-41e8-bc6e-50eae4ef7945

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