FDA Inspection 1102410 — Katja Sockel

Katja Sockel — FEI 3015356560

The FDA completed an inspection of Katja Sockel on August 16, 2019 in Dresden. 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
August 16, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Dresden (Germany)

Additional Details

Clinical Investigator (CI)