# FDA Inspection 901350 - Augmenix Inc - October 17, 2014

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

> FDA Inspection 901350 for Augmenix Inc on October 17, 2014. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 762778 - 2012-01-12](https://www.keypedia.com/records/fda_inspections/augmenix-inc/a32dd3ee-3f1a-4731-8a45-3099faa76af7)

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