FDA Inspection
Neurometrix, Inc.Neurometrix, Inc. – FDA Inspection, May 7, 2015
Record Details
This FDA Inspection record concerns Neurometrix, Inc., with an inspection on May 7, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Neurometrix, Inc.
- Inspection Date
- May 7, 2015
- Product Type
- Devices
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ID · d71eae5b-450c-4e55-a45c-120876debe26
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 929228
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.25(b)Training records
- 21 CFR 820.30(h)Incorrect translation to production specifications
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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 |
| March 20, 2012 | 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 773749 - 2012-03-20
- FDA Inspection 578341 - 2009-04-23
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