FDA Inspection 1274689 — Andrew Moyes, M.D.

Andrew Moyes, M.D. — FEI 3037737000

The FDA completed an inspection of Andrew Moyes, M.D. on June 26, 2025 in Kansas City, MO. 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
June 26, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Kansas City, MO (United States)

Additional Details

Clinical Investigator (CI)