FDA Inspection 1322630 — Timothy Pluard, M.D.

Timothy Pluard, M.D. — FEI 3043914789

The FDA completed an inspection of Timothy Pluard, M.D. on Jun 12, 2026 in Kansas City, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 12, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Kansas City, MO (United States)

Additional Details

Clinical Investigator (CI)