FDA Inspection 1243054 — Jacob DeLaRosa, MD

Jacob DeLaRosa, MD — FEI 3011627108

The FDA completed an inspection of Jacob DeLaRosa, MD on Jun 28, 2024 in Pocatello, ID. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 28, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Pocatello, ID (United States)

Additional Details

Clinical Investigator (CI)