FDA Inspection 1199790 — Ultragenyx Pharmaceutical Inc.

Ultragenyx Pharmaceutical Inc. — FEI 3012208691

The FDA completed an inspection of Ultragenyx Pharmaceutical Inc. on February 27, 2023 in Novato, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 27, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Novato, CA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)