FDA Inspection 1199722 — Louise M Thurman/IPS Research Company

Louise M Thurman/IPS Research Company — FEI 3001701592

The FDA completed an inspection of Louise M Thurman/IPS Research Company on March 8, 2023 in Oklahoma City, OK. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 8, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Oklahoma City, OK (United States)

Additional Details

Clinical Investigator (CI)