FDA Inspection 679383 — Astute
The FDA completed an inspection of Astute on September 8, 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
- September 8, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- West Lebanon, NH (United States)