FDA Inspection 1269921 — Revance Therapeutics, Inc.

Revance Therapeutics, Inc. — FEI 3019604545

The FDA completed an inspection of Revance Therapeutics, Inc. on May 1, 2025 in Moffett Field, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
May 1, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Moffett Field, CA (United States)

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