FDA Inspection 1098947 — Abbott Molecular, Inc.

Abbott Molecular, Inc. — FEI 3005248192

The FDA completed an inspection of Abbott Molecular, Inc. on Jul 10, 2019 in Des Plaines, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 10, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Des Plaines, IL (United States)

Additional Details

Postmarket Audit Inspections

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