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FDA Warning Letter — Neomedix Corporation

Case 420853 — FEI 3003698071

The FDA took a Warning Letter action against Neomedix Corporation on February 26, 2014 (Tustin, CA). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Neomedix Corporation
Date
February 26, 2014
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Tustin, CA (United States)

Facility

Recent inspections

  • 1098182 (NAI Wed Jun 19 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 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))

FDA data resources