FDA Inspection 639896 — Medefil Incorporated
The FDA completed an inspection of Medefil Incorporated on Feb 11, 2010 in Glendale Heights, 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
- Feb 11, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Glendale Heights, IL (United States)