FDA Inspection 1114490 — Ron Waksman

Ron Waksman — FEI 3002932551

The FDA completed an inspection of Ron Waksman on December 10, 2019 in Washington, DC. 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
December 10, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Washington, DC (United States)

Additional Details

Clinical Investigator (CI)