FDA Inspection 1301430 — Erika A. Petersen, M.D.

Erika A. Petersen, M.D. — FEI 3009740152

The FDA completed an inspection of Erika A. Petersen, M.D. on January 30, 2026 in Little Rock, AR. 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
January 30, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Little Rock, AR (United States)

Additional Details

Clinical Investigator (CI)