FDA Inspection 766384 — Subcon Manufacturing Corporation
The FDA completed an inspection of Subcon Manufacturing Corporation on Jan 31, 2012 in Crystal Lake, IL. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI)
- End Date
- Jan 31, 2012
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Crystal Lake, IL (United States)