FDA Inspection 556767 — MGS Manufacturing

MGS Manufacturing — FEI 3004515078

The FDA completed an inspection of MGS Manufacturing on January 14, 2009 in Antioch, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 14, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Antioch, IL (United States)