# NDX Thayer – FDA Inspection, Feb 1, 2018

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

> FDA inspection 1040691 of NDX Thayer, February 01, 2018. Classification: Voluntary Action Indicated (VAI). 8 citations under 21 CFR part 820. Form 483 issued.

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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)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 8

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/jacob-m-dyer/e3ca27e3-e0b1-4db8-9cbe-cfaff90b83cf)

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

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