FDA Inspection 1158759 — Allure Labs, LLC

Allure Labs, LLC — FEI 3000204079

The FDA completed an inspection of Allure Labs, LLC on Dec 3, 2021 in Hayward, CA. 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). 4 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 3, 2021
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hayward, CA (United States)

Citations

IDCFRDescription
110521 CFR 211.22(d)Procedures not in writing, fully followed
127021 CFR 211.68(b)input/output verification
188521 CFR 211.165(b)Microbiological testing
356121 CFR 211.56(b)Written sanitation procedures lacking

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