FDA Inspection
Neurometrix, Inc.Neurometrix, Inc. – FDA Inspection, Mar 20, 2012
Record Details
This FDA Inspection record concerns Neurometrix, Inc., with an inspection on March 20, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Neurometrix, Inc.
- Inspection Date
- March 20, 2012
- Product Type
- Devices
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ID · 2e5bb1f0-5635-4206-ab9e-7a248bc4261b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 773749
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.184DHR content
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Neurometrix, Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| May 27, 2026 | Not classified | New Jersey District Office | Compliance: Devices |
| November 15, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 7, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| May 7, 2015 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 23, 2009 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Neurometrix, Inc.
- FDA Inspection 1319250 - 2026-05-27
- FDA Inspection 1032529 - 2017-11-15
- FDA Inspection 929229 - 2015-05-07
- FDA Inspection 929228 - 2015-05-07
- FDA Inspection 578341 - 2009-04-23
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