FDA Inspection
Hanuri Distribution IncHanuri Distribution Inc – FDA Inspection, Dec 9, 2013
Record Details
This FDA Inspection record concerns Hanuri Distribution Inc, with an inspection on December 9, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Hanuri Distribution Inc
- Inspection Date
- December 9, 2013
- Product Type
- Devices
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ID · 9dcbcaf1-c420-4555-a5ae-5ff8ff177fad
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 859363
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
4- 21 CFR 820.40Lack of procedures, or not maintained
- 21 CFR 820.72(a)Equipment control activity documentation
- 21 CFR 820.80(d)Lack of or inadequate final acceptance procedures
- 21 CFR 803.17Lack of Written MDR Procedures
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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 |
| November 9, 2016 | 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 996932 - 2016-11-09
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