FDA Inspection 557386 — AbbVie Inc.

AbbVie Inc. — FEI 3010166391

The FDA completed an inspection of AbbVie Inc. on Jan 16, 2009 in Wyandotte, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 16, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Wyandotte, MI (United States)

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