FDA Inspection 1013090 — Abbott Molecular, Inc.

Abbott Molecular, Inc. — FEI 3005248192

The FDA completed an inspection of Abbott Molecular, Inc. on May 4, 2017 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
May 4, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Des Plaines, IL (United States)

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