FDA Inspection 945110 — Ameer Kabour MD

Ameer Kabour MD — FEI 3011774421

The FDA completed an inspection of Ameer Kabour MD on September 30, 2015 in Toledo, OH. 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
September 30, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Toledo, OH (United States)

Additional Details

Clinical Investigator (CI)