FDA Inspection 1052858 — Jean Panneton, MD

Jean Panneton, MD — FEI 3014232616

The FDA completed an inspection of Jean Panneton, MD on May 7, 2018 in Norfolk, VA. 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 7, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Norfolk, VA (United States)

Additional Details

Clinical Investigator (CI)