# Dynarex Corporation – FDA Inspection, Mar 2, 2017

Source: https://www.keypedia.com/records/fda_inspections/dynarex-corporation/d9f02058-88a3-4ffb-8942-59d6cb8fdea0
Source feed: FDA_Inspections

> FDA inspection 1005494 of Dynarex Corporation, March 02, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1005494
- Company Name: Dynarex Corporation
- Inspection Date: 2017-03-02
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 1102050 - 2018-11-16](https://www.keypedia.com/records/fda_inspections/dynarex-corporation/436a4b0d-3a2d-48ef-9367-0c0a3947fc49)
- [FDA Inspection 873247 - 2014-03-31](https://www.keypedia.com/records/fda_inspections/dynarex-corporation/6589409d-ab00-4105-8028-80baa9aab4dc)
- FDA Inspection 762080 - 2011-12-20
- [FDA Inspection 567627 - 2009-02-20](https://www.keypedia.com/records/fda_inspections/dynarex-corporation/75335cc0-eda5-40be-adff-26ea15aadde1)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/kwong-p-lee/f4778925-1fad-4988-9e39-86482896c4fa)

Company: https://www.keypedia.com/companies/dynarex-corporation/d0ad5d28-76a3-455f-9f9a-7e55d93edced

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