FDA Inspection 1111725 — Christopher Gilmore MD

Christopher Gilmore MD — FEI 3015781785

The FDA completed an inspection of Christopher Gilmore MD on November 7, 2019 in Winston Salem, NC. 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
November 7, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Winston Salem, NC (United States)

Additional Details

Clinical Investigator (CI)