FDA Warning Letter — Abbott Molecular, Inc.

Case 70264 — FEI 3005248192

The FDA took a Warning Letter action against Abbott Molecular, Inc. on Aug 12, 2009 (Des Plaines, IL). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Abbott Molecular, Inc.
Date
Aug 12, 2009
Fiscal Year
2009
Product Type
Devices
Center
CDRH
Location
Des Plaines, IL (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.