FDA Inspection 684062 — Astute
The FDA completed an inspection of Astute on October 1, 2010 in West Lebanon, NH. 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
- October 1, 2010
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- West Lebanon, NH (United States)
Additional Details
Sponsor, Contract Research Organization