FDA Inspection 985808 — Ostund, Dr Richard

Ostund, Dr Richard — FEI 3007704849

The FDA completed an inspection of Ostund, Dr Richard on Sep 20, 2016 in Saint Louis, MO. 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
Sep 20, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Saint Louis, MO (United States)

Additional Details

Clinical Investigator (CI)