Inspection classificationInspection ended August 21, 2026
FDA inspection of Neurotron, Inc.: VAI
Voluntary action indicated
FDA classified an inspection of Neurotron, Inc. in Aurora, CO as VAI (voluntary action indicated). The inspection ended on August 21, 2026. Product type: Devices.
On the record
- Establishment
- Neurotron, Inc.
- Location
- Aurora, CO
- Classification
- VAI · Voluntary action indicated
- Inspection ended
- 2026-08-21
- Product type
- Devices
- Fiscal year
- FY2026
- FDA establishment identifier (FEI)
- 1121806
- Source
- FDA Data Dashboard ↗
The full record
An account shows the project areas inspected and whether citations were posted.
What an inspection classification is
After an inspection FDA classifies the outcome. NAI (no action indicated): no objectionable conditions were found, or none that justify further action. VAI (voluntary action indicated): objectionable conditions were found, but the agency is not prepared to take or recommend regulatory action. OAI (official action indicated): regulatory or administrative action is recommended.
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From FDA Data Dashboard; FDA posts a classification after its review, which can be months after the inspection ended. The record may have changed since it was read.
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