FDA Inspection 880007 — Robert D. Winslow, M.D.

Robert D. Winslow, M.D. — FEI 3010384025

The FDA completed an inspection of Robert D. Winslow, M.D. on May 15, 2014 in Danbury, CT. 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
May 15, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Danbury, CT (United States)

Additional Details

Clinical Investigator (CI)