# Kaz USA, Inc. – FDA Inspection, Jul 1, 2013

Source: https://www.keypedia.com/records/fda_inspections/kaz-usa-inc/e3e51767-b6d4-49cc-a7f6-f3c45140bcce
Source feed: FDA_Inspections

> FDA inspection 838795 of Kaz USA, Inc., July 01, 2013. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803 and 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 838795
- Company Name: Kaz USA, Inc.
- Inspection Date: 2013-07-01
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- [FDA Inspection 719245 - 2011-04-12](https://www.keypedia.com/records/fda_inspections/kaz-usa-inc/6722527e-3423-41c6-9eb5-937e6594b518)

Company: https://www.keypedia.com/companies/kaz-usa-inc/7b30f71d-06c9-4aef-91ee-5b10d674cd1e

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