FDA Inspection 1005229 — Tommy M Mook Md

Tommy M Mook Md — FEI 3008415613

The FDA completed an inspection of Tommy M Mook Md on Mar 16, 2017 in Shreveport, LA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 16, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Shreveport, LA (United States)

Additional Details

Clinical Investigator (CI)