FDA Inspection 896544 — Neomedix Corporation

Neomedix Corporation — FEI 3003698071

The FDA completed an inspection of Neomedix Corporation on September 19, 2014 in Tustin, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 19, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Tustin, CA (United States)

Citations

IDCFRDescription
1471421 CFR 820.30(c)Design input - Lack of or inadequate procedures