FDA Inspection
Kaz USA, Inc.Kaz USA, Inc. – FDA Inspection, Apr 12, 2011
Record Details
This FDA Inspection record concerns Kaz USA, Inc., with an inspection on April 12, 2011, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Kaz USA, Inc.
- Inspection Date
- April 12, 2011
- Product Type
- Devices
View Company Profile
ID · 6722527e-3423-41c6-9eb5-937e6594b518
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 719245
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
FDA Citations
4- 21 CFR 803.56Submission of Supplement to Individual Report Within One Month
- 21 CFR 820.198(c)Investigation of device failures
- 21 CFR 820.160(a)Lack of or inadequate procedures for distribution
- 21 CFR 820.100(a)Lack of or inadequate procedures
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Other FDA inspections of Kaz USA, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| July 1, 2013 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
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