# Neurotron. Inc. – FDA Inspection, Sep 27, 2010

Source: https://www.keypedia.com/records/fda_inspections/neurotron-inc/ba0cf9a7-db26-4ed3-9eb6-06f5a9da3608
Source feed: FDA_Inspections

> FDA inspection 682551 of Neurotron. Inc., September 27, 2010. Classification: No Action Indicated (NAI). 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 682551
- Company Name: Neurotron. Inc.
- Inspection Date: 2010-09-27
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1007463 - 2017-04-10](https://www.keypedia.com/records/fda_inspections/neurotron-inc/d5eb77a3-b73a-45c2-8cb9-19f2eb582e13)
- [FDA Inspection 1007462 - 2017-04-10](https://www.keypedia.com/records/fda_inspections/neurotron-inc/9041e86f-115b-42ec-99ba-3dace46b3dfd)
- FDA Inspection 799351 - 2012-09-18
- FDA Inspection 798374 - 2012-09-12
- FDA Inspection 554398 - 2008-12-17

Company: https://www.keypedia.com/companies/neurotron-inc/2f572ad6-cb5f-4096-bd37-b1facb33774c

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7