FDA Inspection
Avazzia, IncAvazzia, Inc – FDA Inspection, Aug 30, 2017
Record Details
This FDA Inspection record concerns Avazzia, Inc, with an inspection on August 30, 2017, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 4fa8f75c-c4d1-4abd-a0a5-f8fed8c04a9b
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1023770
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
3- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
- 21 CFR 820.70(c)Environmental control Lack of or inadequate procedures
- 21 CFR 820.80(e)Documentation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Avazzia, Inc
1| Date | Classification | Office | Project area |
|---|---|---|---|
| July 13, 2010 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Avazzia, Inc
- FDA Inspection 673136 - 2010-07-13
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