FDA Inspection 1122516 — Batelle Corporate Operations IRB

Batelle Corporate Operations IRB — FEI 3007895853

The FDA completed an inspection of Batelle Corporate Operations IRB on February 28, 2020 in Columbus, OH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 28, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Columbus, OH (United States)

Additional Details

IRB