FDA Inspection 1020678 — Philipp Harter

Philipp Harter — FEI 3013353642

The FDA completed an inspection of Philipp Harter on June 22, 2017 in Essen. 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
June 22, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Essen (Germany)

Additional Details

Clinical Investigator (CI)