FDA Inspection 872249 — Subcon Manufacturing Corporation

Subcon Manufacturing Corporation — FEI 3004715583

The FDA completed an inspection of Subcon Manufacturing Corporation on Mar 31, 2014 in Crystal Lake, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 31, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Crystal Lake, IL (United States)