FDA Inspection 554398 — Neurotron. Inc.
The FDA completed an inspection of Neurotron. Inc. on December 17, 2008 in Aurora, CO. 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
- December 17, 2008
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Aurora, CO (United States)