FDA Inspection
Viatek Consumer Products Group, Inc.Viatek Consumer Products Group, Inc. – FDA Inspection, Jan 27, 2009
Record Details
This FDA Inspection record concerns Viatek Consumer Products Group, Inc., with an inspection on January 27, 2009, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- January 27, 2009
- Product Type
- Devices
View Company Profile
ID · ed6a6374-62eb-49b9-8eba-d1c3981bd2a0
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 563042
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Viatek Consumer Products Group, Inc.
1| Date | Classification | Office | Project area |
|---|---|---|---|
| May 9, 2017 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Viatek Consumer Products Group, Inc.
- FDA Inspection 1011332 - 2017-05-09
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