FDA Inspection 893517 — Bausch & Lomb, Incorporated

Bausch & Lomb, Incorporated — FEI 1000305478

The FDA completed an inspection of Bausch & Lomb, Incorporated on Aug 13, 2014 in Lynchburg, VA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Aug 13, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Lynchburg, VA (United States)