FDA Inspection
Viltechmeda UABViltechmeda UAB – FDA Inspection, Jan 23, 2012
Record Details
This FDA Inspection record concerns Viltechmeda UAB, with an inspection on January 23, 2012, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Viltechmeda UAB
- Inspection Date
- January 23, 2012
- Product Type
- Devices
View Company Profile
ID · 5aa50482-cff7-4cc2-b31f-2d2b546a45ea
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 763752
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
7- 21 CFR 820.181DMR - not or inadequately maintained
- 21 CFR 820.100(b)Documentation
- 21 CFR 820.40Lack of procedures, or not maintained
- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 820.25(b)Training - Lack of or inadequate procedures
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
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Other FDA inspections of Viltechmeda UAB
1| Date | Classification | Office | Project area |
|---|---|---|---|
| April 30, 2018 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
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