FDA Inspection 783107 — The Estee Lauder Inc.

The Estee Lauder Inc. — FEI 2418643

The FDA completed an inspection of The Estee Lauder Inc. on May 25, 2012 in Melville, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 3 citations were issued during this inspection. Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
May 25, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Melville, NY (United States)

Citations

IDCFRDescription
116221 CFR 211.28(a)Protective Apparel Not Worn
261921 CFR 211.198(b)(2)Complaint Investigation/Follow-Up Findings
438821 CFR 211.198(a)Complaints reviewed by Quality Control Unit

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