FDA Inspection 1311200 — David E. Burdette, M.D.

David E. Burdette, M.D. — FEI 3042663531

The FDA completed an inspection of David E. Burdette, M.D. on March 25, 2026 in Grand Rapids, MI. 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
March 25, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Grand Rapids, MI (United States)

Additional Details

Clinical Investigator (CI)