FDA Inspection 1277227 — Ultragenyx Pharmaceutical Inc.

Ultragenyx Pharmaceutical Inc. — FEI 3012208691

The FDA completed an inspection of Ultragenyx Pharmaceutical Inc. on Jul 17, 2025 in Novato, 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
Jul 17, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Novato, CA (United States)

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