FDA Warning Letter — Customed, Inc.

Case 440230 — FEI 2648727

The FDA took a Warning Letter action against Customed, Inc. on December 9, 2014 (Fajardo, PR). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Customed, Inc.
Date
December 9, 2014
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Fajardo, PR (United States)