# FDA Inspection 1051402 - Viltechmeda UAB - April 30, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/viltechmeda-uab/fe085e93-1988-4a83-9b43-1b33cc659c0a/
Source feed: FDA_Inspections

> FDA Inspection 1051402 for Viltechmeda UAB on April 30, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1051402
- Company Name: Viltechmeda UAB
- Inspection Date: 2018-04-30
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1051402 - 2018-04-30](https://www.globalkeysolutions.net/api/records/fda_inspections/viltechmeda-uab/dd83eef5-0948-4b37-9629-c15c7ce93975/)
- [FDA Inspection 763752 - 2012-01-23](https://www.globalkeysolutions.net/api/records/fda_inspections/viltechmeda-uab/5aa50482-cff7-4cc2-b31f-2d2b546a45ea/)
- [FDA Inspection 763752 - 2012-01-23](https://www.globalkeysolutions.net/api/records/fda_inspections/viltechmeda-uab/59742346-c9cf-446b-a722-fb51a7a8a10a/)

Company: https://www.globalkeysolutions.net/companies/viltechmeda-uab/6735baad-d297-4e78-9127-221451ebc7ec

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7