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FDA Inspection 1098182 — Neomedix Corporation

Neomedix Corporation — FEI 3003698071

The FDA completed an inspection of Neomedix Corporation on June 19, 2019 in Tustin, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 19, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Tustin, CA (United States)

Facility

Other inspections at this facility

  • 1047029 (VAI Thu Mar 29 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 896544 (NAI Fri Sep 19 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 761781 (VAI Thu Dec 29 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources