FDA Inspection 1083796 — Marianne Brodmann, MD

Marianne Brodmann, MD — FEI 3014866095

The FDA completed an inspection of Marianne Brodmann, MD on March 22, 2019 in Graz. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 22, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Graz (Austria)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
297421 CFR 812.110(b)Investigator non-compliance with agreement/plan/regulations