FDA Inspection 1102181 — Timothy M. Koehler, DO

Timothy M. Koehler, DO — FEI 3015457377

The FDA completed an inspection of Timothy M. Koehler, DO on August 30, 2019 in Wichita, KS. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 30, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Wichita, KS (United States)

Additional Details

Clinical Investigator (CI)