# FDA Inspection 1060879 - Kentec Medical, Inc - July 30, 2018

Source: https://www.keypedia.com/records/fda_inspections/kentec-medical-inc/51ee98b0-08eb-4a4c-8843-8adee4db1cd4
Source feed: FDA_Inspections

> FDA Inspection 1060879 for Kentec Medical, Inc on July 30, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1060879
- Company Name: Kentec Medical, Inc
- Inspection Date: 2018-07-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1060879 - 2018-07-30](https://www.keypedia.com/records/fda_inspections/kentec-medical-inc/53a53752-8517-4022-8a6e-43817f29509a)
- [FDA Inspection 928285 - 2015-05-11](https://www.keypedia.com/records/fda_inspections/kentec-medical-inc/9f028993-8233-420b-a20c-4515a3a955ba)
- [FDA Inspection 897383 - 2014-09-24](https://www.keypedia.com/records/fda_inspections/kentec-medical-inc/61acad48-4363-442a-b434-deeb57281a4d)
- [FDA Inspection 897383 - 2014-09-24](https://www.keypedia.com/records/fda_inspections/kentec-medical-inc/bd5ba38e-f756-41fa-a386-defecb57535c)
- [FDA Inspection 803967 - 2012-10-19](https://www.keypedia.com/records/fda_inspections/kentec-medical-inc/324479b0-7d23-47ab-9e05-c450f5e54889)

Company: https://www.keypedia.com/companies/kentec-medical-inc/84a3c6bd-182a-4acd-bf51-a7482ed87bd7

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