FDA Inspection 1112595 — Ines Guttmann-Bauman MD

Ines Guttmann-Bauman MD — FEI 3015893859

The FDA completed an inspection of Ines Guttmann-Bauman MD on December 12, 2019 in Portland, OR. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 12, 2019
Fiscal Year
2020
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Portland, OR (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
753021 CFR 312.62(b)Case history records- inadequate or inadequate
756021 CFR 312.60FD-1572, protocol compliance