FDA Inspection 850039 — James W. Baker, MD

James W. Baker, MD — FEI 3008260036

The FDA completed an inspection of James W. Baker, MD on September 19, 2013 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
September 19, 2013
Fiscal Year
2013
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