FDA Inspection 1095685 — Andrea Rodenbeck

Andrea Rodenbeck — FEI 3015205429

The FDA completed an inspection of Andrea Rodenbeck on Jun 7, 2019 in Kassel. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jun 7, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Kassel (Germany)

Additional details

Clinical Investigator (CI)

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