FDA Inspection 728793 — Novellus Systems, Inc.

Novellus Systems, Inc. — FEI 3005734715

The FDA completed an inspection of Novellus Systems, Inc. on May 23, 2011 in Phoenix, AZ. 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: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 23, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Phoenix, AZ (United States)