FDA Inspection 1233203 — Genentech, Inc.

Genentech, Inc. — FEI 2917293

The FDA completed an inspection of Genentech, Inc. on March 12, 2024 in South San Francisco, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 12, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
South San Francisco, CA (United States)

Additional Details

Sponsor, Contract Research Organization

Citations

IDCFRDescription
745221 CFR 312.56(c)IND safety report
745921 CFR 312.57(a)Records of receipt, shipment, disposition
748221 CFR 312.50General responsibilities of sponsors