FDA Inspection 1143487 — Laura A. Kooienga, M.D.

Laura A. Kooienga, M.D. — FEI 3018301372

The FDA completed an inspection of Laura A. Kooienga, M.D. on May 21, 2021 in Denver, CO. 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
May 21, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Denver, CO (United States)

Additional Details

Clinical Investigator (CI)