# FDA Inspection 793599 - Abryrx, Inc. - July 06, 2012

Source: https://www.keypedia.com/records/fda_inspections/abryrx-inc/83756a74-1050-432d-b217-1f1ee26cad36
Source feed: FDA_Inspections

> FDA Inspection 793599 for Abryrx, Inc. on July 06, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 793599
- Company Name: Abryrx, Inc.
- Inspection Date: 2012-07-06
- Classification: No Action Indicated (NAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 681951 - 2010-09-09](https://www.keypedia.com/records/fda_inspections/abryrx-inc/35d31e67-f8d5-44d2-9946-aa6042fd2b66)

Company: https://www.keypedia.com/companies/abryrx-inc/b904e0a9-997f-48fe-97f8-dd735570ff39

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