# FDA Inspection 1079221 - Cogent Technology, Ltd. - February 14, 2019

Source: https://www.keypedia.com/records/fda_inspections/cogent-technology-ltd/64f9b93b-b919-4f54-aa1c-145c20439762
Source feed: FDA_Inspections

> FDA Inspection 1079221 for Cogent Technology, Ltd. on February 14, 2019. Classification: Voluntary Action Indicated (VAI).

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

## Related Documents

- [FDA Inspection 1002324 - 2017-02-08](https://www.keypedia.com/records/fda_inspections/cogent-technology-ltd/b500e94a-ff16-4138-9990-f07617c46558)

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