FDA Inspection 655888 — Johnson & Johnson Surgical Vision Inc

Johnson & Johnson Surgical Vision Inc — FEI 3003843509

The FDA completed an inspection of Johnson & Johnson Surgical Vision Inc on March 30, 2010 in Santa Ana, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 30, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Santa Ana, CA (United States)