FDA Inspection 1045907 — Ottumwa Regional Health IRB

Ottumwa Regional Health IRB — FEI 3012854181

The FDA completed an inspection of Ottumwa Regional Health IRB on Mar 28, 2018 in Ottumwa, IA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 28, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Ottumwa, IA (United States)

Additional Details

IRB