# Viper Technologies, LLC dba Avalign Thortex – FDA Inspection, Jan 25, 2013

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

> FDA inspection 818020 of Viper Technologies, LLC dba Avalign Thortex, January 25, 2013. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- FDA Inspection 1153939 - 2021-09-24
- [FDA Inspection 967911 - 2016-04-01](https://www.keypedia.com/records/fda_inspections/viper-technologies-llc-dba-avalign-thortex/9e0f4a50-5d7d-4391-8623-24f6bcb39674)
- FDA Inspection 680877 - 2010-09-17

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

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