FDA Inspection 1231324 — Kirsten Watson Alcorn, M.D.

Kirsten Watson Alcorn, M.D. — FEI 3029432082

The FDA completed an inspection of Kirsten Watson Alcorn, M.D. on Feb 22, 2024 in Renton, WA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 22, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Renton, WA (United States)

Additional Details

Clinical Investigator (CI)

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