# Augmenix Inc – FDA Inspection, Oct 17, 2014

Source: https://www.keypedia.com/records/fda_inspections/augmenix-inc/26ec868d-6d6d-4668-8576-3cff6eb1d8aa
Source feed: FDA_Inspections

> FDA inspection 901350 of Augmenix Inc, October 17, 2014. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 901350
- Company Name: Augmenix Inc
- Inspection Date: 2014-10-17
- 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: 2

## Related Documents

- [FDA Inspection 1159303 - 2019-05-22](https://www.keypedia.com/records/fda_inspections/augmenix-inc/8ff429ba-7511-46f0-acd0-ef2824338c3a)
- FDA Inspection 762778 - 2012-01-12

Company: https://www.keypedia.com/companies/augmenix-inc/7abffa27-95c3-4b20-9bab-07f92a0656f9

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