FDA Inspection 1251896 — Beverly Tucker Woodson

Beverly Tucker Woodson — FEI 3030628690

The FDA completed an inspection of Beverly Tucker Woodson on Aug 23, 2024 in Milwaukee, WI. 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
Aug 23, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Milwaukee, WI (United States)

Additional Details

Clinical Investigator (CI)