FDA Inspection 680551 — Genentech, Inc.

Genentech, Inc. — FEI 3006129086

The FDA completed an inspection of Genentech, Inc. on Sep 15, 2010 in Oceanside, 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
Sep 15, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Oceanside, CA (United States)