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FDA Inspection 1263719 — Cornelis Verhoef, MD

Cornelis Verhoef, MD — FEI 3033178969

The FDA completed an inspection of Cornelis Verhoef, MD on Feb 14, 2025 in Rotterdam. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 14, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Rotterdam (Netherlands)

Additional Details

Clinical Investigator (CI)

Facility

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.