FDA Inspection 1267149 — Deborah G. Ristvedt, D.O.

Deborah G. Ristvedt, D.O. — FEI 3035145119

The FDA completed an inspection of Deborah G. Ristvedt, D.O. on April 4, 2025 in Alexandria, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 4, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Alexandria, MN (United States)

Additional Details

Clinical Investigator (CI)