FDA Inspection 921919 — Bausch & Lomb Incorporated

Bausch & Lomb Incorporated — FEI 3003434767

The FDA completed an inspection of Bausch & Lomb Incorporated on March 12, 2015 in Irvine, CA. 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
March 12, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Irvine, CA (United States)