FDA Inspection 1049904 — Exelixis, Inc.

Exelixis, Inc. — FEI 3006375488

The FDA completed an inspection of Exelixis, Inc. on March 27, 2018 in Alameda, 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
March 27, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Alameda, CA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)