FDA Inspection 590120 — Bausch & Lomb Inc

Bausch & Lomb Inc — FEI 1051854

The FDA completed an inspection of Bausch & Lomb Inc on May 6, 2009 in Woodruff, SC. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 6, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Woodruff, SC (United States)