FDA Warning Letter — Cagenix Inc.

Case 233534 — FEI 3007273295

The FDA took a Warning Letter action against Cagenix Inc. on October 24, 2011 (Memphis, TN). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Cagenix Inc.
Date
October 24, 2011
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Memphis, TN (United States)