# FDA Inspection 832499 - Auxogyn Inc. - May 29, 2013

Source: https://www.keypedia.com/records/fda_inspections/auxogyn-inc/2bcd322f-1706-4047-b8b0-2881445aa6a5
Source feed: FDA_Inspections

> FDA Inspection 832499 for Auxogyn Inc. on May 29, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 832499
- Company Name: Auxogyn Inc.
- Inspection Date: 2013-05-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 980999 - 2016-06-01](https://www.keypedia.com/records/fda_inspections/auxogyn-inc/6d2006f2-0bd3-4b91-a704-1511701529dc)
- [FDA Inspection 832499 - 2013-05-29](https://www.keypedia.com/records/fda_inspections/auxogyn-inc/21078163-7360-4ff7-a21f-4311020b6305)

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