FDA Inspection 1116176 — Robert S. Iwaoka, M.D.

Robert S. Iwaoka, M.D. — FEI 3006451762

The FDA completed an inspection of Robert S. Iwaoka, M.D. on January 16, 2020 in Charlotte, NC. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 16, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Charlotte, NC (United States)

Additional Details

Clinical Investigator (CI)