# Neomedix Corporation – FDA Inspection, Mar 29, 2018

Source: https://www.keypedia.com/records/fda_inspections/neomedix-corporation/d4346570-ae2d-4318-9e89-2f29cc46695d
Source feed: FDA_Inspections

> FDA inspection 1047029 of Neomedix Corporation, March 29, 2018. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR parts 806 and 820. Form 483 issued. 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1047029
- Company Name: Neomedix Corporation
- Inspection Date: 2018-03-29
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

## Related Documents

- FDA Inspection 1098182 - 2019-06-19
- FDA Inspection 896544 - 2014-09-19
- [FDA Inspection 761781 - 2011-12-29](https://www.keypedia.com/records/fda_inspections/neomedix-corporation/74102939-e837-40dd-8f06-305e85a4cf2b)

## Related Officers

- Issuing Officer
- [Issuing Officer](https://www.keypedia.com/people/kirtida-patel/c62852cf-9724-4296-bc4b-de8993dcf716)

Company: https://www.keypedia.com/companies/neomedix-corporation/4c7ebf26-90bd-4090-9d8d-12b641ea60a5

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