FDA Inspection 798374 — Neurotron. Inc.
The FDA completed an inspection of Neurotron. Inc. on September 12, 2012 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
- September 12, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Aurora, CO (United States)