FDA Inspection 1134650 — Batelle Corporate Operations IRB
The FDA completed an inspection of Batelle Corporate Operations IRB on December 8, 2020 in Columbus, OH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- December 8, 2020
- Fiscal Year
- 2021
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Columbus, OH (United States)