FDA Inspection
Alan Neuromedical TechnologiesAlan Neuromedical Technologies – FDA Inspection, Sep 13, 2018
Record Details
This FDA Inspection record concerns Alan Neuromedical Technologies, with an inspection on September 13, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 9e57ab8a-5783-433c-a40e-28cc49face0e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1066052
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 820.198(a)Complaints
- 21 CFR 820.22Quality Audit/Reaudit - conducted
- 21 CFR 820.50(a)(1)Evaluation and Selection, Suppliers, Contractors, etc.
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Other FDA inspections of Alan Neuromedical Technologies
2| Date | Classification | Office | Project area |
|---|---|---|---|
| November 5, 2014 | OAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| April 8, 2011 | OAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
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