FDA Inspection 1117659 — Portola Pharmaceuticals, Inc.

Portola Pharmaceuticals, Inc. — FEI 3004737419

The FDA completed an inspection of Portola Pharmaceuticals, Inc. on December 17, 2019 in South San Francisco, 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
December 17, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
South San Francisco, CA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)