FDA Inspection 911396 — Bausch & Lomb Incorporated

Bausch & Lomb Incorporated — FEI 1032500

The FDA completed an inspection of Bausch & Lomb Incorporated on January 15, 2015 in Greenville, 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
January 15, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Greenville, SC (United States)