FDA Inspection 1068242 — David Grainger, M.D.

David Grainger, M.D. — FEI 3014489724

The FDA completed an inspection of David Grainger, M.D. on Aug 30, 2018 in Wichita, KS. 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
Aug 30, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Wichita, KS (United States)

Additional Details

Clinical Investigator (CI)