FDA Inspection
Neurometrix, Inc.Neurometrix, Inc. – FDA Inspection, Apr 23, 2009
Record Details
This FDA Inspection record concerns Neurometrix, Inc., with an inspection on April 23, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Neurometrix, Inc.
- Inspection Date
- April 23, 2009
- Product Type
- Devices
View Company Profile
ID · 7968d24c-6db3-4598-ab41-51e2d9214c6d
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 578341
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
2- 21 CFR 820.198(e)Maintained
- 21 CFR 803.17Lack of Written MDR Procedures
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 |
| March 20, 2012 | VAI | Center for Devices and Radiological Health | Compliance: 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 773749 - 2012-03-20
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.