# Auxogyn Inc. – FDA Inspection, Jun 1, 2016

Source: https://www.keypedia.com/records/fda_inspections/auxogyn-inc/6d2006f2-0bd3-4b91-a704-1511701529dc
Source feed: FDA_Inspections

> FDA inspection 980999 of Auxogyn Inc., June 01, 2016. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 980999
- Company Name: Auxogyn Inc.
- Inspection Date: 2016-06-01
- 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: 1

## Related Documents

- [FDA Inspection 832499 - 2013-05-29](https://www.keypedia.com/records/fda_inspections/auxogyn-inc/2bcd322f-1706-4047-b8b0-2881445aa6a5)

Company: https://www.keypedia.com/companies/auxogyn-inc/0d128072-b474-4f2e-b244-4aad557d9b21

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