FDA Inspection 1042694 — Elizabeth Arden, Inc.

Elizabeth Arden, Inc. — FEI 3013779173

The FDA completed an inspection of Elizabeth Arden, Inc. on Feb 15, 2018 in Salem, VA. 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
Feb 15, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Salem, VA (United States)

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