FDA Warning Letter — Nomax, Inc.

Case 512566 — FEI 1937310

The FDA took a Warning Letter action against Nomax, Inc. on December 15, 2016 (Saint Louis, MO). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Nomax, Inc.
Date
December 15, 2016
Fiscal Year
2017
Product Type
Devices
Center
CDRH
Location
Saint Louis, MO (United States)