# Azog, Inc. – FDA Inspection, Dec 16, 2009

Source: https://www.keypedia.com/records/fda_inspections/azog-inc/e6a6a1f0-213b-4cd4-ac16-5d8854fe738e
Source feed: FDA_Inspections

> FDA inspection 635936 of Azog, Inc., December 16, 2009. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 635936
- Company Name: Azog, Inc.
- Inspection Date: 2009-12-16
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1159384 - 2021-11-09
- FDA Inspection 1026174 - 2017-08-08
- FDA Inspection 780677 - 2012-05-10

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

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