FDA Inspection 1277662 — Laura A. Kooienga, M.D.

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

The FDA completed an inspection of Laura A. Kooienga, M.D. on Jul 28, 2025 in Denver, CO. 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
Jul 28, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Denver, CO (United States)

Additional Details

Clinical Investigator (CI)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.