# Cogent Technology, Ltd. – FDA Inspection, Feb 14, 2019

Source: https://www.keypedia.com/records/fda_inspections/cogent-technology-ltd/a8e95bb9-44ae-49e8-a6c7-2d7bbef809e0
Source feed: FDA_Inspections

> FDA inspection 1079221 of Cogent Technology, Ltd., February 14, 2019. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1079221
- Company Name: Cogent Technology, Ltd.
- Inspection Date: 2019-02-14
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1002324 - 2017-02-08

## Related Officers

- [Company Rep](https://www.keypedia.com/people/roy-baby/69a18ef5-167c-41eb-a57e-3d138a0820c2)

Company: https://www.keypedia.com/companies/cogent-technology-ltd/9a110bf1-2c4c-40b8-8e1d-acb98ff6a84f

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