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FDA Inspection 585721 — Allure Labs, LLC

Allure Labs, LLC — FEI 3000204079

The FDA completed an inspection of Allure Labs, LLC on May 20, 2009 in Hayward, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 20, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hayward, CA (United States)

Facility

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Recent compliance actions

FDA data resources