FDA Inspection 1065396 — David R. Liljenquist, M.D.

David R. Liljenquist, M.D. — FEI 3007946708

The FDA completed an inspection of David R. Liljenquist, M.D. on Aug 3, 2018 in Idaho Falls, 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
Aug 3, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Idaho Falls, ID (United States)

Additional Details

Clinical Investigator (CI)