FDA Inspection 1070226 — Amy G. Brenner, M.D.

Amy G. Brenner, M.D. — FEI 3014721523

The FDA completed an inspection of Amy G. Brenner, M.D. on October 4, 2018 in Mason, 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
October 4, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Mason, OH (United States)

Additional Details

Clinical Investigator (CI)