FDA Inspection 1084927 — Kyle Coleman, M.D.

Kyle Coleman, M.D. — FEI 3015097868

The FDA completed an inspection of Kyle Coleman, M.D. on March 20, 2019 in New Orleans, LA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 20, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
New Orleans, LA (United States)

Additional Details

Clinical Investigator (CI)