# FDA Inspection 1032529 - Neurometrix, Inc. - November 15, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/neurometrix-inc/1ef19bc6-17f5-4a10-8b7e-a6f6c1f6e0e5
Source feed: FDA_Inspections

> FDA Inspection 1032529 for Neurometrix, Inc. on November 15, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1032529
- Company Name: Neurometrix, Inc.
- Inspection Date: 2017-11-15
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1032529 - 2017-11-15](https://www.globalkeysolutions.net/records/fda_inspections/neurometrix-inc/5a11058b-449b-48a5-b4ed-7f4ca09db699)
- [FDA Inspection 929228 - 2015-05-07](https://www.globalkeysolutions.net/records/fda_inspections/neurometrix-inc/d71eae5b-450c-4e55-a45c-120876debe26)
- [FDA Inspection 929229 - 2015-05-07](https://www.globalkeysolutions.net/records/fda_inspections/neurometrix-inc/0b0f6083-170a-48ba-9122-aa5ef50135f3)
- [FDA Inspection 773749 - 2012-03-20](https://www.globalkeysolutions.net/records/fda_inspections/neurometrix-inc/2e5bb1f0-5635-4206-ab9e-7a248bc4261b)
- [FDA Inspection 578341 - 2009-04-23](https://www.globalkeysolutions.net/records/fda_inspections/neurometrix-inc/4292541c-0955-416a-b161-79b5095cd407)

Company: https://www.globalkeysolutions.net/companies/neurometrix-inc/415c4be9-8f3f-4225-855b-3c72aa169773

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