# FDA Inspection 1100444 - Volex Inc - August 26, 2019

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

> FDA Inspection 1100444 for Volex Inc on August 26, 2019. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1100444 - 2019-08-26](https://www.keypedia.com/records/fda_inspections/volex-inc/09ec7572-1051-48c1-bd78-418c5eeed4ce)

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