FDA Inspection
Neurodynamics, Inc.Neurodynamics, Inc. – FDA Inspection, Oct 4, 2017
Record Details
This FDA Inspection record concerns Neurodynamics, Inc., with an inspection on October 4, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · c6a5f13e-c7ec-4143-b52f-79d369494fa3
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1027756
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.30(a)Design control - no procedures
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Other FDA inspections of Neurodynamics, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| February 28, 2024 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| July 21, 2021 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Neurodynamics, Inc.
- FDA Inspection 1231517 - 2024-02-28
- FDA Inspection 1146691 - 2021-07-21
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