FDA Inspection 1029783 — S. DiSean Kendall, M.D.

S. DiSean Kendall, M.D. — FEI 3013558065

The FDA completed an inspection of S. DiSean Kendall, M.D. on September 1, 2017 in Salt Lake City, UT. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 1, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Salt Lake City, UT (United States)

Additional Details

Clinical Investigator (CI)