# Neomedix Corporation, Tustin, CA – FDA Inspections

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

> Inspection records and compliance data for Neomedix Corporation in Tustin, California. 4 FDA inspections on record, 1 Form 483, 1 warning letter, last inspected June 19, 2019.

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## Details

- Name: Neomedix Corporation
- FEI Number: 3003698071
- Address Line 1: 15042 Parkway Loop Ste A
- City: Tustin
- State: California
- Zip Code: 92780
- Country Name: United States
- Address: 15042 Parkway Loop Ste A, Tustin, California 92780, United States
- Country: United States

## Related Documents

- [WARNING_LETTER - Neomedix Corporation - Unknown Date](https://www.keypedia.com/records/warning_letter/neomedix-corporation/ab28fd8f-5c90-41f5-9674-7f7c42944b61) — source: FDA, date: Invalid Date
- FDA Inspection 1098182 - Neomedix Corporation - 2019-06-19 — classification: No Action Indicated (NAI), source: FDA, date: June 19, 2019
- FDA Inspection 1098182 - Neomedix Corporation - 2019-06-19 — classification: No Action Indicated (NAI), source: FDA, date: June 19, 2019
- FDA Inspection 1047029 - Neomedix Corporation - 2018-03-29 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 29, 2018
- [FDA Inspection 1047029 - Neomedix Corporation - 2018-03-29](https://www.keypedia.com/records/fda_inspections/neomedix-corporation/d4346570-ae2d-4318-9e89-2f29cc46695d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 29, 2018
- FDA Inspection 896544 - Neomedix Corporation - 2014-09-19 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 19, 2014
- FDA Inspection 896544 - Neomedix Corporation - 2014-09-19 — classification: No Action Indicated (NAI), source: FDA, date: September 19, 2014
- [FDA Inspection 761781 - Neomedix Corporation - 2011-12-29](https://www.keypedia.com/records/fda_inspections/neomedix-corporation/74102939-e837-40dd-8f06-305e85a4cf2b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 29, 2011

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