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FDA Inspection 1009391 — Gilbert Upchurch, MD

Gilbert Upchurch, MD — FEI 3012861465

The FDA completed an inspection of Gilbert Upchurch, MD on Jan 27, 2017 in Charlottesville, 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
Jan 27, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Charlottesville, VA (United States)

Additional Details

Clinical Investigator (CI)

Facility

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.