FDA Inspection 1115372 — Hendrik Gerrit van der Poel

Hendrik Gerrit van der Poel — FEI 3015648493

The FDA completed an inspection of Hendrik Gerrit van der Poel on November 15, 2019 in Amsterdam. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 15, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Amsterdam (Netherlands)

Additional Details

Clinical Investigator (CI)