FDA Inspection 791162 — Genentech, Inc.

Genentech, Inc. — FEI 3007232634

The FDA completed an inspection of Genentech, Inc. on Jun 27, 2012 in Hillsboro, OR. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 27, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hillsboro, OR (United States)