# AZ Instrument (Shen Zhen) Co., Ltd. – FDA Inspection, Nov 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 of AZ Instrument (Shen Zhen) Co., Ltd., November 11, 2010. Classification: Official Action Indicated (OAI). 2 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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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)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 891964 - 2014-07-16

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