# FDA Inspection 1026174 - Azog, Inc. - August 08, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/azog-inc/d9e5e862-d8b3-4e4e-ae11-87ac6b26db79
Source feed: FDA_Inspections

> FDA Inspection 1026174 for Azog, Inc. on August 08, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1026174
- Company Name: Azog, Inc.
- Inspection Date: 2017-08-08
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/azog-inc/bd04cf82-6602-4656-a18a-2b501659973b

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