FDA Inspection 1247729 — Keith Xavier, M.D.

Keith Xavier, M.D. — FEI 3031091304

The FDA completed an inspection of Keith Xavier, M.D. on Aug 9, 2024 in Arlington, TX. 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
Aug 9, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Arlington, TX (United States)

Additional Details

Clinical Investigator (CI)