# FDA Inspection 1022786 - MedTrak VNG, Inc. - July 26, 2017

Source: https://www.keypedia.com/records/fda_inspections/medtrak-vng-inc/24a28cd5-003e-47b1-8ab0-cee1de8a7b83
Source feed: FDA_Inspections

> FDA Inspection 1022786 for MedTrak VNG, Inc. on July 26, 2017. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1022786
- Company Name: MedTrak VNG, Inc.
- Inspection Date: 2017-07-26
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1022786 - 2017-07-26](https://www.keypedia.com/records/fda_inspections/medtrak-vng-inc/2c5cf976-58b4-4405-8eb1-4815ad262f4f)
- [FDA Inspection 822284 - 2013-03-22](https://www.keypedia.com/records/fda_inspections/medtrak-vng-inc/ce791125-5386-4978-a3e1-788ecc0caaa3)

Company: https://www.keypedia.com/companies/medtrak-vng-inc/60970303-c260-4ebc-96c7-715f372d71aa

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