# FDA Inspection 704298 - AZ Instrument (Shen Zhen) Co., Ltd. - November 11, 2010

Source: https://www.keypedia.com/records/fda_inspections/az-instrument-shen-zhen-co-ltd/56520099-e9e0-4227-abcf-6c0be04d12dd
Source feed: FDA_Inspections

> FDA Inspection 704298 for AZ Instrument (Shen Zhen) Co., Ltd. on November 11, 2010. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 704298
- Company Name: AZ Instrument (Shen Zhen) Co., Ltd.
- Inspection Date: 2010-11-11
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 891964 - 2014-07-16](https://www.keypedia.com/records/fda_inspections/az-instrument-shen-zhen-co-ltd/122bf57b-8aa9-4dba-9f35-9ea822b45dd7)
- [FDA Inspection 891964 - 2014-07-16](https://www.keypedia.com/records/fda_inspections/az-instrument-shen-zhen-co-ltd/e7ba6cd2-179b-4be7-9668-0468d37d217d)

Company: https://www.keypedia.com/companies/az-instrument-shen-zhen-co-ltd/3155234b-1e66-4405-9091-7d83362ad84f

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