FDA Inspection
Neurotron. Inc.Neurotron. Inc. – FDA Inspection, Sep 27, 2010
Record Details
This FDA Inspection record concerns Neurotron. Inc., with an inspection on September 27, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Neurotron. Inc.
- Inspection Date
- September 27, 2010
- Product Type
- Devices
View Company Profile
ID · ba0cf9a7-db26-4ed3-9eb6-06f5a9da3608
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 682551
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Neurotron. Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| April 10, 2017 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| April 10, 2017 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 18, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 12, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 17, 2008 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Neurotron. Inc.
- FDA Inspection 1007463 - 2017-04-10
- FDA Inspection 1007462 - 2017-04-10
- FDA Inspection 799351 - 2012-09-18
- FDA Inspection 798374 - 2012-09-12
- FDA Inspection 554398 - 2008-12-17
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