FDA Inspection 608320 — WCG IRB, Inc
The FDA completed an inspection of WCG IRB, Inc on Aug 21, 2009 in Puyallup, WA. 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: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Aug 21, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Puyallup, WA (United States)
Additional Details
IRB