FDA Inspection 1262486 — Revance Therapeutics, Inc

Revance Therapeutics, Inc — FEI 3007772056

The FDA completed an inspection of Revance Therapeutics, Inc on Feb 27, 2025 in Newark, 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). 1 citation was issued during this inspection. Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 27, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Newark, CA (United States)

Citations

IDCFRDescription
360321 CFR 211.160(b)Scientifically sound laboratory controls

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