# FDA Inspection 1040691 - NDX Thayer - February 01, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/ndx-thayer/fa2fdb5e-9cbf-49ab-a3c4-ac12a27ef535/
Source feed: FDA_Inspections

> FDA Inspection 1040691 for NDX Thayer on February 01, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1040691
- Company Name: NDX Thayer
- Inspection Date: 2018-02-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1040691 - 2018-02-01](https://www.globalkeysolutions.net/api/records/fda_inspections/ndx-thayer/b04303d1-a8fa-45a6-81fc-a88994dba010/)

Company: https://www.globalkeysolutions.net/companies/ndx-thayer/e4ab71c6-280c-4233-8aa4-603468502cfc

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