# Dexta Corporation – FDA Inspection, Feb 3, 2015

Source: https://www.keypedia.com/records/fda_inspections/dexta-corporation/cb514bbd-c4d9-4875-b5cb-3787919f442f
Source feed: FDA_Inspections

> FDA inspection 910140 of Dexta Corporation, February 03, 2015. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 910140
- Company Name: Dexta Corporation
- Inspection Date: 2015-02-03
- 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: 7

## Related Documents

- [FDA Inspection 869842 - 2014-03-06](https://www.keypedia.com/records/fda_inspections/dexta-corporation/54d0be4a-af99-4187-8e0c-8050522d8591)
- [FDA Inspection 663287 - 2010-05-26](https://www.keypedia.com/records/fda_inspections/dexta-corporation/ed5c4c55-6d57-4780-888e-eb7f29678a56)

Company: https://www.keypedia.com/companies/dexta-corporation/3c9ac744-9e9d-4d43-ae97-05f69adfad1e

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