FDA Inspection 639721 — Genentech, Inc.

Genentech, Inc. — FEI 3007232634

The FDA completed an inspection of Genentech, Inc. on Dec 17, 2009 in Hillsboro, OR. 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
Dec 17, 2009
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hillsboro, OR (United States)