# FDA Inspection 818020 - Viper Technologies, LLC dba Avalign Thortex - January 25, 2013

Source: https://www.globalkeysolutions.net/records/fda_inspections/viper-technologies-llc-dba-avalign-thortex/faa1005d-5760-41bd-b33b-127eb8ab5563/
Source feed: FDA_Inspections

> FDA Inspection 818020 for Viper Technologies, LLC dba Avalign Thortex on January 25, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 818020
- Company Name: Viper Technologies, LLC dba Avalign Thortex
- Inspection Date: 2013-01-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/viper-technologies-llc-dba-avalign-thortex/f7cc4d02-fded-4c8a-a1bc-f9e522ca8839

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