FDA Inspection 1018471 — Dirk-Jan Slebos, MD, PhD

Dirk-Jan Slebos, MD, PhD — FEI 3013488052

The FDA completed an inspection of Dirk-Jan Slebos, MD, PhD on June 23, 2017 in Groningen. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 23, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Groningen (Netherlands)

Additional Details

Clinical Investigator (CI)