FDA Inspection 1106051 — Jacob W. Zeiders III, M.D.

Jacob W. Zeiders III, M.D. — FEI 3015487713

The FDA completed an inspection of Jacob W. Zeiders III, M.D. on September 24, 2019 in Fort Lauderdale, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 24, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Fort Lauderdale, FL (United States)

Additional Details

Clinical Investigator (CI)