FDA Inspection 1061624 — Kevin B. Kaiserman, M.D.

Kevin B. Kaiserman, M.D. — FEI 3014289226

The FDA completed an inspection of Kevin B. Kaiserman, M.D. on Jun 20, 2018 in Torrance, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 20, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Torrance, CA (United States)

Additional Details

Clinical Investigator (CI)