FDA Inspection 926019 — Danny H. Sugimoto, M.D.

Danny H. Sugimoto, M.D. — FEI 3007207764

The FDA completed an inspection of Danny H. Sugimoto, M.D. on May 20, 2015 in Chicago, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 20, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Chicago, IL (United States)

Additional Details

Clinical Investigator (CI)