FDA Inspection 1032043 — Harald Vogelsang

Harald Vogelsang — FEI 3013663601

The FDA completed an inspection of Harald Vogelsang on Oct 13, 2017 in Vienna. 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
Oct 13, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Vienna (Austria)

Additional Details

Clinical Investigator (CI)

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