FDA Warning Letter — Subcon Manufacturing Corporation

Case 375498 — FEI 3004715583

The FDA took a Warning Letter action against Subcon Manufacturing Corporation on Dec 16, 2013 (Crystal Lake, IL). The action was issued by CDRH and concerns devices products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Subcon Manufacturing Corporation
Date
Dec 16, 2013
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Crystal Lake, IL (United States)