FDA Inspection 596362 — Abbott Molecular, Inc.

Abbott Molecular, Inc. — FEI 3005248192

The FDA completed an inspection of Abbott Molecular, Inc. on June 29, 2009 in Des Plaines, IL. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
June 29, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Des Plaines, IL (United States)