FDA Inspection 1096743 — Mary Kay, Inc

Mary Kay, Inc — FEI 1618579

The FDA completed an inspection of Mary Kay, Inc on Jul 19, 2019 in Dallas, TX. 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
Jul 19, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dallas, TX (United States)

Citations

IDCFRDescription
122021 CFR 211.67(b)(3)Cleaning SOPs/instructions
179021 CFR 211.80(b)Handling and Storage to Prevent Contamination
179721 CFR 211.82(a)Examination on receipt, before acceptance

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