FDA Inspection 646264 — Kenneth J. Rosenthal, M.D.

Kenneth J. Rosenthal, M.D. — FEI 3003480969

The FDA completed an inspection of Kenneth J. Rosenthal, M.D. on Jan 27, 2010 in Great Neck, NY. 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
Jan 27, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Great Neck, NY (United States)

Additional Details

Clinical Investigator (CI)