# Neomedix Corporation – FDA Inspection, Dec 29, 2011

Source: https://www.keypedia.com/records/fda_inspections/neomedix-corporation/74102939-e837-40dd-8f06-305e85a4cf2b
Source feed: FDA_Inspections

> FDA inspection 761781 of Neomedix Corporation, December 29, 2011. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 761781
- Company Name: Neomedix Corporation
- Inspection Date: 2011-12-29
- 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: 3

## Related Documents

- FDA Inspection 1098182 - 2019-06-19
- [FDA Inspection 1047029 - 2018-03-29](https://www.keypedia.com/records/fda_inspections/neomedix-corporation/d4346570-ae2d-4318-9e89-2f29cc46695d)
- FDA Inspection 896544 - 2014-09-19

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