FDA Inspection 1035275 — Blaise Baxter, M.D.

Blaise Baxter, M.D. — FEI 3013834633

The FDA completed an inspection of Blaise Baxter, M.D. on Nov 29, 2017 in Chattanooga, TN. 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
Nov 29, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Chattanooga, TN (United States)

Additional Details

Clinical Investigator (CI)

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