# Volex Inc – FDA Inspection, Aug 26, 2019

Source: https://www.keypedia.com/records/fda_inspections/volex-inc/ccbc0c8d-2e42-431e-b7b7-e1dc458046ee
Source feed: FDA_Inspections

> FDA inspection 1100444 of Volex Inc, August 26, 2019. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1100444
- Company Name: Volex Inc
- Inspection Date: 2019-08-26
- 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: 1

## Related Officers

- [Wilfred A. Darang](https://www.keypedia.com/people/wilfred-a-darang/f0f1e653-891d-47d6-82e3-5ce40a5d3635)

Company: https://www.keypedia.com/companies/volex-inc/01e799ce-fd32-4332-b6f4-0f78b67f3e23

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