# FDA Inspection 930509 - Auric Enterprises, Inc. D.B.A. Diack - June 17, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/auric-enterprises-inc-dba-diack/62de23da-b293-4159-9238-897d781aa804
Source feed: FDA_Inspections

> FDA Inspection 930509 for Auric Enterprises, Inc. D.B.A. Diack on June 17, 2015. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 930509
- Company Name: Auric Enterprises, Inc. D.B.A. Diack
- Inspection Date: 2015-06-17
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 930509 - 2015-06-17](https://www.globalkeysolutions.net/records/fda_inspections/auric-enterprises-inc-dba-diack/9c3e243d-703e-4f3b-aa4b-f0b1f0a28d33)

Company: https://www.globalkeysolutions.net/companies/auric-enterprises-inc-dba-diack/e034321a-4505-4f4a-b090-a9ac1388d1cd

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