FDA Inspection
Hanuri Distribution IncHanuri Distribution Inc – FDA Inspection, Nov 9, 2016
Record Details
This FDA Inspection record concerns Hanuri Distribution Inc, with an inspection on November 9, 2016, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 67d6511d-7c2c-4ba9-8be8-f970c5523b61
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 996932
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 820.184DHR - not or inadequately maintained
- 21 CFR 820.80(d)Lack of or inadequate final acceptance procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Hanuri Distribution Inc
3| Date | Classification | Office | Project area |
|---|---|---|---|
| March 26, 2026 | NAI | Los Angeles District Office | Postmarket Assurance: Medical Devices |
| July 22, 2021 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 9, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Hanuri Distribution Inc
- FDA Inspection 1309458 - 2026-03-26
- FDA Inspection 1147676 - 2021-07-22
- FDA Inspection 859363 - 2013-12-09
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